A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527300



Internal ID15454593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:90685340..90700221hg38UCSC Ensembl
Innerchr6:91395059..91409940hg19UCSC Ensembl
Innerchr6:91451780..91466661hg18UCSC Ensembl
Innerchr6:91451780..91466661hg17UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg3814882
hg1914882
hg1814882
hg1714882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703718
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527300
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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