A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022965



Internal ID19112182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:145053715..145314249hg38UCSC Ensembl
Innerchr6:145374851..145635385hg19UCSC Ensembl
Innerchr6:145416544..145677078hg18UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg38260535
hg19260535
hg18260535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3654457
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)nsv1022965
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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