A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102954



Internal ID20669994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58697908..58706759hg38UCSC Ensembl
chr3:58683635..58692486hg19UCSC Ensembl
Cytoband3p14.2
Allele length
AssemblyAllele length
hg388852
hg198852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6359950
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102954
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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