A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516523



Internal ID15443816
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:144398629..144407196hg38UCSC Ensembl
Innerchr6:144719765..144728332hg19UCSC Ensembl
Innerchr6:144761458..144770025hg18UCSC Ensembl
Innerchr6:144761458..144770025hg17UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg388568
hg198568
hg188568
hg178568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv663087, nssv661698, nssv668858
Samples
Known GenesUTRN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516523
Frequency
Sample Size2026
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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