A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6414414



Internal ID21071967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:132536582..132562185hg38UCSC Ensembl
chr5:131872274..131897877hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg3825604
hg1925604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18127125
Samples
Known GenesIL5, RAD50
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6414414
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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