A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020402



Internal ID19109621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:11647401..11934365hg38UCSC Ensembl
Innerchr9:11647401..11934365hg19UCSC Ensembl
Innerchr9:11637401..11924365hg18UCSC Ensembl
Cytoband9p23
Allele length
AssemblyAllele length
hg38286965
hg19286965
hg18286965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7412n100
Supporting Variantsnssv3758183, nssv3689285, nssv3689282, nssv3689281, nssv3758184, nssv3689284, nssv3689280, nssv3689283
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)nsv1020402
Frequency
Sample Size11257
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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