A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1135474



Internal ID19262894
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:20715859..20725116hg38UCSC Ensembl
Outerchr14:21184018..21193275hg19UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg389258
hg199258
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1052n106
Supporting Variantsnssv3989032
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1135474
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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