A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122981



Internal ID18936058
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:74457385..74457449hg38UCSC Ensembl
Outerchr15:74749726..74749790hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3865
hg1965
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971578
SamplesKWS2
Known GenesUBL7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122981
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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