A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358008



Internal ID21015561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:98471810..98472329hg38UCSC Ensembl
chr3:98190654..98191173hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38520
hg19520
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104924
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358008
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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