A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695539



Internal ID15085505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:24262601..24271450hg38UCSC Ensembl
Innerchr7:24302220..24311069hg19UCSC Ensembl
Innerchr7:24268745..24277594hg18UCSC Ensembl
Innerchr7:24075460..24084309hg17UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg388850
hg198850
hg188850
hg178850
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517053
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695539
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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