A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv702707



Internal ID15439359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:159048203..159075720hg38UCSC Ensembl
Innerchr5:158475211..158502728hg19UCSC Ensembl
Innerchr5:158407789..158435306hg18UCSC Ensembl
Innerchr5:158407789..158435306hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg3827518
hg1927518
hg1827518
hg1727518
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv526407
Supporting Variants
Samples
Known GenesEBF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv702707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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