A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1134095



Internal ID19279883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:77562591..77562710hg38UCSC Ensembl
Outerchr4:78483745..78483864hg19UCSC Ensembl
Cytoband4q21.1
Allele length
AssemblyAllele length
hg38120
hg19120
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3970438
SamplesKWS1
Known GenesCXCL13
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1134095
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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