A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143779



Internal ID18935561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:37099599..37102299hg38UCSC Ensembl
Outerchr15:37391800..37394500hg19UCSC Ensembl
Cytoband15q14
Allele length
AssemblyAllele length
hg382701
hg192701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994474
SamplesKWS1
Known GenesMEIS2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143779
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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