A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv525529



Internal ID15452822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:83530727..83576787hg38UCSC Ensembl
Innerchr3:83579878..83625938hg19UCSC Ensembl
Innerchr3:83662568..83708628hg18UCSC Ensembl
Innerchr3:83662568..83708628hg17UCSC Ensembl
Cytoband3p12.1
Allele length
AssemblyAllele length
hg3846061
hg1946061
hg1846061
hg1746061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv701664
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv525529
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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