A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528924



Internal ID15456217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:181389271..181399661hg38UCSC Ensembl
Innerchr1:181358407..181368797hg19UCSC Ensembl
Innerchr1:179625030..179635420hg18UCSC Ensembl
Innerchr1:178090064..178100454hg17UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg3810391
hg1910391
hg1810391
hg1710391
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705614
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528924
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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