A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702023



Internal ID15438675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:107118353..107128437hg38UCSC Ensembl
Innerchr6:107439557..107449641hg19UCSC Ensembl
Innerchr6:107546250..107556334hg18UCSC Ensembl
Innerchr6:107546250..107556334hg17UCSC Ensembl
Cytoband6q21
Allele length
AssemblyAllele length
hg3810085
hg1910085
hg1810085
hg1710085
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525833
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702023
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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