A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370629



Internal ID21028182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:148336201..148339300hg38UCSC Ensembl
chr3:148053988..148057087hg19UCSC Ensembl
Cytoband3q24
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370629
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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