A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703821



Internal ID15093787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:6148152..6168738hg38UCSC Ensembl
Innerchr7:6187783..6208369hg19UCSC Ensembl
Innerchr7:6154309..6174894hg18UCSC Ensembl
Innerchr7:5961024..5981609hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg3820587
hg1920587
hg1820586
hg1720586
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527386
Supporting Variants
Samples
Known GenesCYTH3, USP42
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703821
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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