A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1004278



Internal ID15951548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:110048416..110061092hg38UCSC Ensembl
Innerchr4:110969572..110982248hg19UCSC Ensembl
Innerchr4:111189021..111201697hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3812677
hg1912677
hg1812677
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv595145
Supporting Variants
Samples
Known GenesELOVL6
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1004278
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer