A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981012



Internal ID19216118
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:92768270..92771370hg38UCSC Ensembl
Outerchr15:93311500..93314600hg19UCSC Ensembl
Cytoband15q26.1
Allele length
AssemblyAllele length
hg383101
hg193101
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118334
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981012
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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