A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021476



Internal ID19110694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11647401..11841788hg38UCSC Ensembl
Innerchr9:11647401..11841788hg19UCSC Ensembl
Innerchr9:11637401..11831788hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38194388
hg19194388
hg18194388
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7413n100
Supporting Variantsnssv3758182
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)nsv1021476
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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