A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv518303



Internal ID15445596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:170254992..170257897hg38UCSC Ensembl
Innerchr6:170564080..170566985hg19UCSC Ensembl
Innerchr6:170406005..170408910hg18UCSC Ensembl
Innerchr6:170481712..170484617hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg382906
hg192906
hg182906
hg172906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695734
Samples
Known GenesLOC154449
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv518303
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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