A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1136335



Internal ID18940595
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr20:63895147..63895547hg38UCSC Ensembl
Outerchr20:62526500..62526900hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg38401
hg19401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3989956
SamplesKWS2
Known GenesDNAJC5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1136335
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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