A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3002198



Internal ID17295150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:133625782..133625865hg38UCSC Ensembl
Outerchr5:132961473..132961556hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3884
hg1984
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955885
Supporting Variants
SamplesBILGI_BIOE
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3002198
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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