A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023822



Internal ID19113039
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:23327657..23358450hg38UCSC Ensembl
Innerchr9:23327655..23358448hg19UCSC Ensembl
Innerchr9:23317655..23348448hg18UCSC Ensembl
Cytoband9p21.3
Allele length
AssemblyAllele length
hg3830794
hg1930794
hg1830794
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3690738
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)nsv1023822
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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