A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6374530



Internal ID21032083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:132229099..132231797hg38UCSC Ensembl
chr3:131947943..131950641hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg382699
hg192699
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094155
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6374530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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