A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981337



Internal ID18860505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98647471..98648671hg38UCSC Ensembl
Outerchr15:99190700..99191900hg19UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg381201
hg191201
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1144746
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981337
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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