A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3538382



Internal ID18836663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20942515hg38UCSC Ensembl
Innerchr15:20262224..21147844hg19UCSC Ensembl
Innerchr15:18522238..19412503hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38885545
hg19885621
hg18890266
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048245
Supporting Variants
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)nssv3538382
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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