A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv526221



Internal ID15106828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:78731939..79021395hg38UCSC Ensembl
Innerchr1:79197624..79487080hg19UCSC Ensembl
Innerchr1:78970212..79259668hg18UCSC Ensembl
Innerchr1:78909645..79199101hg17UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg38289457
hg19289457
hg18289457
hg17289457
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv702486
Samples
Known GenesELTD1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv526221
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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