A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1046494



Internal ID19135713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20818293hg38UCSC Ensembl
Innerchr15:20216943..21023622hg19UCSC Ensembl
Innerchr15:18476957..19283673hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38806604
hg19806680
hg18806717
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2195n100
Supporting Variantsnssv3715762
Samples
Known GenesCHEK2P2, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1046494
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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