A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1039427



Internal ID19128646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20078801..20689298hg38UCSC Ensembl
Innerchr15:20284054..20894627hg19UCSC Ensembl
Innerchr15:18544068..19178339hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38610498
hg19610574
hg18634272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2195n100
Supporting Variantsnssv3536550, nssv3715980
Samples
Known GenesCHEK2P2, GOLGA6L6, GOLGA8CP, HERC2P3, NBEAP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1039427
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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