A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524431



Internal ID15451724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:139202158..139217074hg38UCSC Ensembl
Innerchr6:139523295..139538211hg19UCSC Ensembl
Innerchr6:139564988..139579904hg18UCSC Ensembl
Innerchr6:139564988..139579904hg17UCSC Ensembl
Cytoband6q24.1
Allele length
AssemblyAllele length
hg3814917
hg1914917
hg1814917
hg1714917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700358
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524431
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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