A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18121789



Internal ID20688829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:87670401..87794300hg38UCSC Ensembl
chr4:88591553..88715452hg19UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg38123900
hg19123900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6394018
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18121789
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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