A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3639537



Internal ID18591132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:133995284..134147172hg38UCSC Ensembl
Innerchr4:134916439..135068327hg19UCSC Ensembl
Innerchr4:135135889..135287777hg18UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg38151889
hg19151889
hg18151889
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1015565
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3639537
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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