A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698989



Internal ID15088955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:137176295..137266198hg38UCSC Ensembl
Innerchr4:138097449..138187352hg19UCSC Ensembl
Innerchr4:138316899..138406802hg18UCSC Ensembl
Innerchr4:138455054..138544957hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3889904
hg1989904
hg1889904
hg1789904
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516176
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698989
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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