A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062181



Internal ID18804712
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31960187..34056597hg38UCSC Ensembl
Innerchr16:31971508..33859064hg19UCSC Ensembl
Innerchr16:31879009..33766565hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382096411
hg191887557
hg181887557
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3716189
Samples
Known GenesHERC2P4, LOC390705, RNU6-76P, SLC6A10P, TP53TG3, TP53TG3B, TP53TG3C, TP53TG3D
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062181
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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