A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044806



Internal ID19134025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20235273..20376190hg38UCSC Ensembl
Innerchr15:20440526..20581443hg19UCSC Ensembl
Innerchr15:18700540..18841457hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38140918
hg19140918
hg18140918
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2220n100
Supporting Variantsnssv3539440
Samples
Known GenesCHEK2P2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1044806
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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