A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410214



Internal ID21067767
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:112634734..112635339hg38UCSC Ensembl
chr5:111970431..111971036hg19UCSC Ensembl
Cytoband5q22.2
Allele length
AssemblyAllele length
hg38606
hg19606
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123089
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410214
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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