A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406643



Internal ID21064196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:131173388..131173853hg38UCSC Ensembl
chr5:130509081..130509546hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg38466
hg19466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18125109
Samples
Known GenesLYRM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406643
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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