A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701253



Internal ID15091219
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:9929338..9949081hg38UCSC Ensembl
Innerchr4:9930962..9950705hg19UCSC Ensembl
Innerchr4:9540060..9559803hg18UCSC Ensembl
Innerchr4:9607231..9626974hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3819744
hg1919744
hg1819744
hg1719744
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525177
Supporting Variants
Samples
Known GenesSLC2A9
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701253
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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