A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv661372



Internal ID15051338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150092890..150105136hg38UCSC Ensembl
Innerchr6:150414026..150426272hg19UCSC Ensembl
Innerchr6:150455719..150467965hg18UCSC Ensembl
Innerchr6:150506140..150518386hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3812247
hg1912247
hg1812247
hg1712247
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517022
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv661372
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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