A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139632



Internal ID18904208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73533559..73535959hg38UCSC Ensembl
Outerchr15:73825900..73828300hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg382401
hg192401
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3977218
SamplesKWS2
Known GenesC15orf60
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139632
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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