A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033372



Internal ID19122594
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:93274061..93302887hg38UCSC Ensembl
Innerchr8:94286289..94315115hg19UCSC Ensembl
Innerchr8:94355465..94384291hg18UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3828827
hg1928827
hg1828827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7269n100
Supporting Variantsnssv3689722
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)nsv1033372
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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