A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519219



Internal ID15446512
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:36296150..36317052hg38UCSC Ensembl
Innerchr7:36335759..36356661hg19UCSC Ensembl
Innerchr7:36302284..36323186hg18UCSC Ensembl
Innerchr7:36108999..36129901hg17UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3820903
hg1920903
hg1820903
hg1720903
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696709
Samples
Known GenesEEPD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519219
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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