A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695338



Internal ID15085304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:43029915..43065208hg38UCSC Ensembl
Innerchr15:43322113..43357406hg19UCSC Ensembl
Innerchr15:41109405..41144698hg18UCSC Ensembl
Innerchr15:41109405..41144698hg17UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg3835294
hg1935294
hg1835294
hg1735294
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv515876
Supporting Variants
Samples
Known GenesUBR1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv695338
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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