A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6357687



Internal ID21015240
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:32502201..32503000hg38UCSC Ensembl
chr3:32543693..32544492hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099396
Samples
Known GenesCMTM6
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6357687
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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