A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1044839



Internal ID19134058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20060713..20376190hg38UCSC Ensembl
Innerchr15:20265966..20581443hg19UCSC Ensembl
Innerchr15:18525980..18841457hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38315478
hg19315478
hg18315478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2197n100
Supporting Variantsnssv3538594
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)nsv1044839
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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