A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700621



Internal ID15090587
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9862074..9870851hg38UCSC Ensembl
Innerchr4:9863698..9872475hg19UCSC Ensembl
Innerchr4:9472796..9481573hg18UCSC Ensembl
Innerchr4:9539967..9548744hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg388778
hg198778
hg188778
hg178778
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524654
Supporting Variants
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700621
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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