A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408198



Internal ID21065751
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:52636652..52638667hg38UCSC Ensembl
chr5:51932486..51934501hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg382016
hg192016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133604
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408198
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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