A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680677



Internal ID15417329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:39707188..39709027hg38UCSC Ensembl
Innerchr4:39708808..39710647hg19UCSC Ensembl
Innerchr4:39385203..39387042hg18UCSC Ensembl
Innerchr4:39531374..39533213hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg381840
hg191840
hg181840
hg171840
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516320
Supporting Variants
Samples
Known GenesUBE2K
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680677
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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