A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412575



Internal ID21070128
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:129802828..129804845hg38UCSC Ensembl
chr5:129138521..129140538hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg382018
hg192018
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126163
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412575
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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