A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1052517



Internal ID19141736
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:81110338..81377259hg38UCSC Ensembl
Innerchr9:83725253..83992174hg19UCSC Ensembl
Innerchr9:82915073..83181994hg18UCSC Ensembl
Cytoband9q21.31
Allele length
AssemblyAllele length
hg38266922
hg19266922
hg18266922
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3697520
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1052517
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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