A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143608



Internal ID18940048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:37595195..37595595hg38UCSC Ensembl
Outerchr14:38064400..38064800hg19UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3981291
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143608
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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