A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550278



Internal ID18848559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..32500434hg38UCSC Ensembl
Innerchr16:32146874..32511755hg19UCSC Ensembl
Innerchr16:32054375..32419256hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38364882
hg19364882
hg18364882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064537
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)nssv3550278
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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