A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395588



Internal ID21053141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:159105516..159107655hg38UCSC Ensembl
chr5:158532524..158534663hg19UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg382140
hg192140
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126857
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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