A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv523425



Internal ID15450718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:141752887..141808872hg38UCSC Ensembl
Innerchr6:142074024..142130009hg19UCSC Ensembl
Innerchr6:142115717..142171702hg18UCSC Ensembl
Innerchr6:142115717..142171702hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3855986
hg1955986
hg1855986
hg1755986
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv396n21
Supporting Variantsnssv699180
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv523425
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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