A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058932



Internal ID19148151
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..32513445hg38UCSC Ensembl
Innerchr16:32158595..32524766hg19UCSC Ensembl
Innerchr16:32066096..32432267hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38366172
hg19366172
hg18366172
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2853n100
Supporting Variantsnssv3550331
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)nsv1058932
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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