A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv668844



Internal ID15058810
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:40265863..40301738hg38UCSC Ensembl
Innerchr15:40558064..40593939hg19UCSC Ensembl
Innerchr15:38345356..38381231hg18UCSC Ensembl
Innerchr15:38345356..38381231hg17UCSC Ensembl
Cytoband15q15.1
Allele length
AssemblyAllele length
hg3835876
hg1935876
hg1835876
hg1735876
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517541
Supporting Variants
Samples
Known GenesANKRD63, PAK6, PLCB2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv668844
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