A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366495



Internal ID21024048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:127415344..127440497hg38UCSC Ensembl
chr3:127134187..127159340hg19UCSC Ensembl
Cytoband3q21.3
Allele length
AssemblyAllele length
hg3825154
hg1925154
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094100
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366495
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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