A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519304



Internal ID15446597
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155266287..155287024hg38UCSC Ensembl
Innerchr7:155057997..155078734hg19UCSC Ensembl
Innerchr7:154688930..154709667hg18UCSC Ensembl
Innerchr7:154495645..154516382hg17UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3820738
hg1920738
hg1820738
hg1720738
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv697298, nssv655251, nssv685888, nssv689636
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519304
Frequency
Sample Size2026
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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