A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18102929



Internal ID20669969
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:58178467..58179732hg38UCSC Ensembl
chr3:58164194..58165459hg19UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg381266
hg191266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363116
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18102929
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00072


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