A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv520025



Internal ID15447318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:40320631..40392605hg38UCSC Ensembl
Innerchr3:40362122..40434096hg19UCSC Ensembl
Innerchr3:40337126..40409100hg18UCSC Ensembl
Innerchr3:40337126..40409100hg17UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3871975
hg1971975
hg1871975
hg1771975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697184
Samples
Known GenesENTPD3, ENTPD3-AS1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv520025
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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