A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701666



Internal ID15438318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89860302..89915777hg38UCSC Ensembl
Innerchr7:89489616..89545091hg19UCSC Ensembl
Innerchr7:89327552..89383027hg18UCSC Ensembl
Innerchr7:89134267..89189742hg17UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3855476
hg1955476
hg1855476
hg1755476
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525531
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701666
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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