A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678080



Internal ID15414732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:70113668..70116294hg38UCSC Ensembl
Innerchr4:70979385..70982011hg19UCSC Ensembl
Innerchr4:71013974..71016600hg18UCSC Ensembl
Innerchr4:71160145..71162771hg17UCSC Ensembl
Cytoband4q13.3
Allele length
AssemblyAllele length
hg382627
hg192627
hg182627
hg172627
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517703
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678080
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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