A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064520



Internal ID19153739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32147274..33629681hg38UCSC Ensembl
Innerchr16:32158595..33432148hg19UCSC Ensembl
Innerchr16:32066096..33339649hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg381482408
hg191273554
hg181273554
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2842n100
Supporting Variantsnssv3550349
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1064520
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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