A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035876



Internal ID19125095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20011690..20688370hg38UCSC Ensembl
Innerchr15:20216943..20893699hg19UCSC Ensembl
Innerchr15:18476957..19153713hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38676681
hg19676757
hg18676757
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2186n100
Supporting Variantsnssv3536966, nssv3536964, nssv3536965
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)nsv1035876
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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