A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1057724



Internal ID19146943
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35237438..35526596hg38UCSC Ensembl
Innerchr16:34471809..34760967hg19UCSC Ensembl
Innerchr16:34329310..34618468hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38289159
hg19289159
hg18289159
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558809, nssv3558808, nssv3558813, nssv3558811, nssv3558815, nssv3558801, nssv3558816, nssv3558805, nssv3558807, nssv3558814, nssv3558817, nssv3558810, nssv3558806, nssv3558800, nssv3558802, nssv3558812, nssv3558803, nssv3558804, nssv3722625
Samples
Known GenesLOC100130700, LOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1057724
Frequency
Sample Size11257
Observed Gain19
Observed Loss0
Observed Complex0
Frequencyn/a


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