A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527525



Internal ID15454818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144398629..144416534hg38UCSC Ensembl
Innerchr6:144719765..144737670hg19UCSC Ensembl
Innerchr6:144761458..144779363hg18UCSC Ensembl
Innerchr6:144761458..144779363hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg3817906
hg1917906
hg1817906
hg1717906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703980
Samples
Known GenesUTRN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527525
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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