A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409022



Internal ID21066575
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87314199..87315471hg38UCSC Ensembl
chr5:86610016..86611288hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18136120
Samples
Known GenesRASA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409022
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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