A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526643



Internal ID15107250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161138008..161140224hg38UCSC Ensembl
Innerchr6:161559040..161561256hg19UCSC Ensembl
Innerchr6:161479030..161481246hg18UCSC Ensembl
Innerchr6:161529451..161531667hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg382217
hg192217
hg182217
hg172217
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702969
Samples
Known GenesAGPAT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526643
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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