A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv656365



Internal ID15046331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:144000454..144003245hg38UCSC Ensembl
Innerchr4:144921607..144924398hg19UCSC Ensembl
Innerchr4:145141057..145143848hg18UCSC Ensembl
Innerchr4:145279212..145282003hg17UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg382792
hg192792
hg182792
hg172792
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517006
Supporting Variants
Samples
Known GenesGYPB
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv656365
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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