A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527098



Internal ID15107705
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:161138008..161144126hg38UCSC Ensembl
Innerchr6:161559040..161565158hg19UCSC Ensembl
Innerchr6:161479030..161485148hg18UCSC Ensembl
Innerchr6:161529451..161535569hg17UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg386119
hg196119
hg186119
hg176119
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703477
Samples
Known GenesAGPAT4
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527098
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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