A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524641



Internal ID15451934
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:150304436..150322894hg38UCSC Ensembl
Innerchr6:150625572..150644030hg19UCSC Ensembl
Innerchr6:150667265..150685723hg18UCSC Ensembl
Innerchr6:150717686..150736144hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg3818459
hg1918459
hg1818459
hg1718459
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700607
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524641
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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