A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18041910



Internal ID20608950
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:4635463..4635883hg38UCSC Ensembl
chr18:4635463..4635883hg19UCSC Ensembl
Cytoband18p11.31
Allele length
AssemblyAllele length
hg38421
hg19421
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6529229
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18041910
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00079


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