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nsv4985646

  • Variant Calls:1
  • Validation:Not tested
  • Clinical Assertions: No
  • Region Size:3,704

Links to Other Resources

Source: NCBI

Genome View

Select assembly:
Overlapping variant regions from other studies: 120 SVs from 31 studies. See in: genome view    
Submitted genomic56,262,411-56,266,239Question Mark
Overlapping variant regions from other studies: 120 SVs from 31 studies. See in: genome view    
Remapped(Score: Perfect):56,656,195-56,660,023Question Mark

Variant Region Placement Information

Variant Region IDPlacement TypeScoreAssemblyAssembly UnitReciprocitySequence IDChrStartStop
nsv4985646Submitted genomicGRCh38 (hg38)Primary AssemblyNC_000012.12Chr1256,262,485 (-74, +2)56,266,188 (-2, +51)
nsv4985646RemappedPerfectGRCh37.p13Primary AssemblyFirst PassNC_000012.11Chr1256,656,269 (-74, +2)56,659,972 (-2, +51)

Variant Call Information

Variant Call IDTypeMethodAnalysis
nssv16553734duplicationSequencingSequence alignment

Variant Call Placement Information

Variant Call IDPlacement TypeScoreHGVSAssemblyReciprocitySequence IDChrStartStop
nssv16553734Submitted genomicNC_000012.12:g.(56
262411_56262487)_(
56266186_56266239)
dup
GRCh38 (hg38)NC_000012.12Chr1256,262,485 (-74, +2)56,266,188 (-2, +51)
nssv16553734RemappedPerfectNC_000012.11:g.(56
656195_56656271)_(
56659970_56660023)
dup
GRCh37.p13First PassNC_000012.11Chr1256,656,269 (-74, +2)56,659,972 (-2, +51)

No validation data were submitted for this variant

No clinical assertion data were submitted for this variant

Genotype Information

Variant Call IDAllele Frequency (AF)Allele Count (AC)Allele Number (AN)
nssv16553734<0.001129246
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