A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362572



Internal ID21020125
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:141100445..141102960hg38UCSC Ensembl
chr3:140819287..140821802hg19UCSC Ensembl
Cytoband3q23
Allele length
AssemblyAllele length
hg382516
hg192516
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094286
Samples
Known GenesSPSB4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362572
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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