A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv705373



Internal ID15095339
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:42851800..43065218hg38UCSC Ensembl
Innerchr15:43143998..43357416hg19UCSC Ensembl
Innerchr15:40931290..41144708hg18UCSC Ensembl
Innerchr15:40931290..41144708hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg38213419
hg19213419
hg18213419
hg17213419
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515876
Supporting Variants
Samples
Known GenesTTBK2, UBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv705373
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