A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404262



Internal ID21061815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87323934..87327349hg38UCSC Ensembl
chr5:86619751..86623166hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383416
hg193416
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136122
Samples
Known GenesRASA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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