A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031356



Internal ID19120578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11992592..12205632hg38UCSC Ensembl
Innerchr9:11992592..12205632hg19UCSC Ensembl
Innerchr9:11982592..12195632hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38213041
hg19213041
hg18213041
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7437n100
Supporting Variantsnssv3690535
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)nsv1031356
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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