A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143782



Internal ID19256364
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:62327601..62333501hg38UCSC Ensembl
Outerchr15:62619800..62625700hg19UCSC Ensembl
Cytoband15q22.2
Allele length
AssemblyAllele length
hg385901
hg195901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994477
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143782
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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