A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18131354



Internal ID20698394
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:57827201..57833800hg38UCSC Ensembl
chr5:57123028..57129627hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg386600
hg196600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6404914
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18131354
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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