A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18103781



Internal ID20670821
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72171128..72172659hg38UCSC Ensembl
chr3:72220279..72221810hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg381532
hg191532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6360345
Supporting Variants
Samples
Known GenesLINC00870
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18103781
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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