A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1036005



Internal ID19125224
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr15:20056971..20729850hg38UCSC Ensembl
Innerchr15:20262224..20935179hg19UCSC Ensembl
Innerchr15:18522238..19195186hg18UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg38672880
hg19672956
hg18672949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2201n100
Supporting Variantsnssv3538377
Samples
Known GenesCHEK2P2, 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)nsv1036005
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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