A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6358759



Internal ID21016312
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:163763314..163763926hg38UCSC Ensembl
chr3:163481102..163481714hg19UCSC Ensembl
Cytoband3q26.1
Allele length
AssemblyAllele length
hg38613
hg19613
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095142
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6358759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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