A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524842



Internal ID15452135
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:112569317..112574931hg38UCSC Ensembl
Innerchr6:112890519..112896133hg19UCSC Ensembl
Innerchr6:112997212..113002826hg18UCSC Ensembl
Innerchr6:112997212..113002826hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg385615
hg195615
hg185615
hg175615
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700844
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524842
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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