A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705287



Internal ID15441939
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:148765085..148771525hg38UCSC Ensembl
Innerchr7:148462177..148468617hg19UCSC Ensembl
Innerchr7:148093110..148099550hg18UCSC Ensembl
Innerchr7:147899825..147906265hg17UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg386441
hg196441
hg186441
hg176441
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv528653
Supporting Variants
Samples
Known GenesCUL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705287
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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