A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3551177



Internal ID18849458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32384286..33564608hg38UCSC Ensembl
Innerchr16:32395607..33367075hg19UCSC Ensembl
Innerchr16:32303108..33274576hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381180323
hg19971469
hg18971469
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066576
Supporting Variants
Samples
Known GenesLOC390705, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3551177
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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