A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1113694



Internal ID19252081
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:25943483..25943544hg38UCSC Ensembl
Outerchr15:26188630..26188691hg19UCSC Ensembl
Cytoband15q12
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3969763
SamplesKWS2
Known GenesLOC100128714
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1113694
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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