A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524995



Internal ID15452288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:140412718..140480360hg38UCSC Ensembl
Innerchr6:140733855..140801497hg19UCSC Ensembl
Innerchr6:140775548..140843190hg18UCSC Ensembl
Innerchr6:140775548..140843190hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3867643
hg1967643
hg1867643
hg1767643
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701026
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524995
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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