A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv667950



Internal ID15404602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:153020470..153024858hg38UCSC Ensembl
Innerchr4:153941622..153946010hg19UCSC Ensembl
Innerchr4:154161072..154165460hg18UCSC Ensembl
Innerchr4:154299227..154303615hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg384389
hg194389
hg184389
hg174389
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517491
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv667950
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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