A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038908



Internal ID19128127
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:19998696..20376299hg38UCSC Ensembl
Innerchr15:20203949..20581552hg19UCSC Ensembl
Innerchr15:18463963..18841566hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38377604
hg19377604
hg18377604
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2176n100
Supporting Variantsnssv3534494
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)nsv1038908
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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