A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18127127



Internal ID20694167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132554173..132558438hg38UCSC Ensembl
chr5:131889865..131894130hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg384266
hg194266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6410588
Supporting Variants
Samples
Known GenesRAD50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18127127
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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