A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3550279



Internal ID18848560
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..32603585hg38UCSC Ensembl
Innerchr16:32146874..32614906hg19UCSC Ensembl
Innerchr16:32054375..32522407hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38468033
hg19468033
hg18468033
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059203
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)nssv3550279
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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