A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042822



Internal ID19132041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20538504hg38UCSC Ensembl
Innerchr15:20284054..20743782hg19UCSC Ensembl
Innerchr15:18544068..19003796hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38459704
hg19459729
hg18459729
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2202n100
Supporting Variantsnssv3540044
Samples
Known GenesCHEK2P2, GOLGA6L6, HERC2P3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042822
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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