A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669516



Internal ID15406168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:121421420..121470953hg38UCSC Ensembl
Innerchr4:122342575..122392108hg19UCSC Ensembl
Innerchr4:122562025..122611558hg18UCSC Ensembl
Innerchr4:122700180..122749713hg17UCSC Ensembl
Cytoband4q27
Allele length
AssemblyAllele length
hg3849534
hg1949534
hg1849534
hg1749534
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516606
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669516
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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