A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103760



Internal ID20670800
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:71590204..71593326hg38UCSC Ensembl
chr3:71639355..71642477hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg383123
hg193123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6366038
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103760
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00028


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