A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1138691



Internal ID19256623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:27241131..27260697hg38UCSC Ensembl
Outerchr19:27732039..27751605hg19UCSC Ensembl
Cytoband19q11
Allele length
AssemblyAllele length
hg3819567
hg1919567
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3991278
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1138691
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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