A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059977



Internal ID18802508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:31963377..33970586hg38UCSC Ensembl
Innerchr16:31974698..33773053hg19UCSC Ensembl
Innerchr16:31882199..33680554hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg382007210
hg191798356
hg181798356
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2840n100
Supporting Variantsnssv3549186, nssv3716190
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)nsv1059977
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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