A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134791



Internal ID18910446
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:38832413..38832465hg38UCSC Ensembl
Outerchr19:39323053..39323105hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3853
hg1953
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3972677, nssv3971268
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134791
Frequency
Sample Size2
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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