A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404451



Internal ID21062004
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:51732204..51732725hg38UCSC Ensembl
chr5:51028038..51028559hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38522
hg19522
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404451
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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