A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682911



Internal ID15419563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:160426213..160585745hg38UCSC Ensembl
Innerchr4:161347365..161506897hg19UCSC Ensembl
Innerchr4:161566815..161726347hg18UCSC Ensembl
Innerchr4:161704970..161864502hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg38159533
hg19159533
hg18159533
hg17159533
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv521144
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682911
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