A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516122



Internal ID15443415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103634120..103651378hg38UCSC Ensembl
Innerchr7:103274567..103291825hg19UCSC Ensembl
Innerchr7:103061803..103079061hg18UCSC Ensembl
Innerchr7:102868518..102885776hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3817259
hg1917259
hg1817259
hg1717259
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv695828, nssv679907, nssv666355
Samples
Known GenesRELN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516122
Frequency
Sample Size2026
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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