A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694571



Internal ID15084537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:100398008..100400607hg38UCSC Ensembl
Innerchr4:101319165..101321764hg19UCSC Ensembl
Innerchr4:101538188..101540787hg18UCSC Ensembl
Innerchr4:101676343..101678942hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg382600
hg192600
hg182600
hg172600
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521801
Supporting Variants
Samples
Known GenesEMCN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694571
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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