A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361169



Internal ID21018722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:102762808..102763244hg38UCSC Ensembl
chr3:102481652..102482088hg19UCSC Ensembl
Cytoband3q12.3
Allele length
AssemblyAllele length
hg38437
hg19437
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18091186
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361169
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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