A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18126265



Internal ID20693305
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:136441182..136441737hg38UCSC Ensembl
chr5:135776871..135777426hg19UCSC Ensembl
Cytoband5q31.1
Allele length
AssemblyAllele length
hg38556
hg19556
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6399583
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18126265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00072


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