A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv521391



Internal ID15448684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:10018741..10048089hg38UCSC Ensembl
Innerchr3:10060425..10089773hg19UCSC Ensembl
Innerchr3:10035425..10064773hg18UCSC Ensembl
Innerchr3:10035425..10064773hg17UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3829349
hg1929349
hg1829349
hg1729349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv698000
Samples
Known GenesCIDECP, FANCD2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv521391
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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