A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359122



Internal ID21016675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:95634113..95634598hg38UCSC Ensembl
chr3:95352957..95353442hg19UCSC Ensembl
Cytoband3q11.2
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104052
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359122
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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