A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032533



Internal ID19121755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:80566036..80584685hg38UCSC Ensembl
Innerchr6:81275753..81294402hg19UCSC Ensembl
Innerchr6:81332472..81351121hg18UCSC Ensembl
Cytoband6q14.1
Allele length
AssemblyAllele length
hg3818650
hg1918650
hg1818650
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6073n100
Supporting Variantsnssv3648817
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)nsv1032533
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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