A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042684



Internal ID18785215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:8897997..9125030hg38UCSC Ensembl
Innerchr16:8991854..9218887hg19UCSC Ensembl
Innerchr16:8899355..9126388hg18UCSC Ensembl
Cytoband16p13.2
Allele length
AssemblyAllele length
hg38227034
hg19227034
hg18227034
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2725n100
Supporting Variantsnssv3557113
Samples
Known GenesC16orf72, USP7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042684
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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