A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1122889



Internal ID19254144
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:35375550..35375612hg38UCSC Ensembl
Outerchr14:35844756..35844818hg19UCSC Ensembl
Cytoband14q13.2
Allele length
AssemblyAllele length
hg3863
hg1963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3971484
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1122889
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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