A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056156



Internal ID19145375
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:35237438..35499505hg38UCSC Ensembl
Innerchr16:34471809..34733876hg19UCSC Ensembl
Innerchr16:34329310..34591377hg18UCSC Ensembl
Cytoband16p11.1
Allele length
AssemblyAllele length
hg38262068
hg19262068
hg18262068
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2962n100
Supporting Variantsnssv3558714
Samples
Known GenesLOC146481, LOC283914
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056156
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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