A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18095961



Internal ID20663001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146137761..146193592hg38UCSC Ensembl
chr3:145855548..145911379hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg3855832
hg1955832
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6363739
Supporting Variants
Samples
Known GenesPLOD2, PLSCR4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18095961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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