A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525755



Internal ID15453048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:167190659..167209340hg38UCSC Ensembl
Innerchr6:167604147..167622828hg19UCSC Ensembl
Innerchr6:167524137..167542818hg18UCSC Ensembl
Innerchr6:167574558..167593239hg17UCSC Ensembl
Cytoband6q27
Allele length
AssemblyAllele length
hg3818682
hg1918682
hg1818682
hg1718682
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701923
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525755
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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