A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6385202



Internal ID21042755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:20626828..20746040hg38UCSC Ensembl
chr5:20626937..20746149hg19UCSC Ensembl
Cytoband5p14.3
Allele length
AssemblyAllele length
hg38119213
hg19119213
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130369
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6385202
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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