A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701146



Internal ID15437798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:5917982..5924824hg38UCSC Ensembl
Innerchr4:5919709..5926551hg19UCSC Ensembl
Innerchr4:5970610..5977452hg18UCSC Ensembl
Innerchr4:6037781..6044623hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg386843
hg196843
hg186843
hg176843
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525088
Supporting Variants
Samples
Known GenesMIR378D1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701146
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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