A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056746



Internal ID19145965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32169453..32904180hg38UCSC Ensembl
Innerchr16:32180774..32915501hg19UCSC Ensembl
Innerchr16:32088275..32823002hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38734728
hg19734728
hg18734728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2841n100
Supporting Variantsnssv3716301
Samples
Known GenesLOC390705, 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)nsv1056746
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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