A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369757



Internal ID21027310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:157518184..157519354hg38UCSC Ensembl
chr3:157235973..157237143hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg381171
hg191171
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096530
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369757
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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