A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067501



Internal ID19156720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..32603585hg38UCSC Ensembl
Innerchr16:32158595..32614906hg19UCSC Ensembl
Innerchr16:32066096..32522407hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38456312
hg19456312
hg18456312
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2850n100
Supporting Variantsnssv3550332
Samples
Known GenesHERC2P4, LOC390705, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1067501
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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