A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698742



Internal ID15435394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:54152450..54179549hg38UCSC Ensembl
Innerchr4:55018617..55045716hg19UCSC Ensembl
Innerchr4:54713374..54740473hg18UCSC Ensembl
Innerchr4:54859545..54886644hg17UCSC Ensembl
Cytoband4q12
Allele length
AssemblyAllele length
hg3827100
hg1927100
hg1827100
hg1727100
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523058
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698742
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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