A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3716297



Internal ID19014578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..32421720hg38UCSC Ensembl
Innerchr16:32158595..32433041hg19UCSC Ensembl
Innerchr16:32066096..32340542hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38274447
hg19274447
hg18274447
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1060577
Supporting Variants
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)nssv3716297
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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