A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037080



Internal ID19126299
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20240873..20952464hg38UCSC Ensembl
Innerchr15:20446126..21157793hg19UCSC Ensembl
Innerchr15:18706140..19422452hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38711592
hg19711668
hg18716313
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2222n100
Supporting Variantsnssv3534738, nssv3534737, nssv3534736
Samples
Known GenesCHEK2P2, CT60, CXADRP2, GOLGA6L6, GOLGA8CP, HERC2P3, LOC646214, NBEAP1, NF1P2, POTEB, POTEB2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037080
Frequency
Sample Size11257
Observed Gain2
Observed Loss1
Observed Complex0
Frequencyn/a


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