A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058667



Internal ID18801198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31960187..32401900hg38UCSC Ensembl
Innerchr16:31971508..32413221hg19UCSC Ensembl
Innerchr16:31879009..32320722hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38441714
hg19441714
hg18441714
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2835n100
Supporting Variantsnssv3549169
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)nsv1058667
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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