A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1067239



Internal ID19156458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:32135553..32832367hg38UCSC Ensembl
Innerchr16:32146874..32843688hg19UCSC Ensembl
Innerchr16:32054375..32751189hg18UCSC Ensembl
Cytoband16p11.2
Allele length
AssemblyAllele length
hg38696815
hg19696815
hg18696815
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2841n100
Supporting Variantsnssv3550293
Samples
Known GenesHERC2P4, LOC390705, 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)nsv1067239
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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