A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516060



Internal ID15443353
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:104977871..104981955hg38UCSC Ensembl
Innerchr7:104618318..104622402hg19UCSC Ensembl
Innerchr7:104405554..104409638hg18UCSC Ensembl
Innerchr7:104212269..104216353hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg384085
hg194085
hg184085
hg174085
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv692072, nssv665939
Samples
Known GenesLINC01004
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516060
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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