A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6356755



Internal ID21014308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:189926301..189927100hg38UCSC Ensembl
chr3:189644090..189644889hg19UCSC Ensembl
Cytoband3q28
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18100590
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6356755
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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