A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv694176



Internal ID15430828
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:183049873..183089564hg38UCSC Ensembl
Innerchr4:183971026..184010717hg19UCSC Ensembl
Innerchr4:184208020..184247711hg18UCSC Ensembl
Innerchr4:184346175..184385866hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3839692
hg1939692
hg1839692
hg1739692
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517885
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv694176
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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