A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18122676



Internal ID20689716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:103776993..103778555hg38UCSC Ensembl
chr5:103112694..103114256hg19UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg381563
hg191563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6403212
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18122676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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