A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362571



Internal ID21020124
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:146630887..146631496hg38UCSC Ensembl
chr3:146348674..146349283hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg38610
hg19610
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096190
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362571
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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