A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363455



Internal ID21021008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115422681..115463683hg38UCSC Ensembl
chr3:115141528..115182530hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3841003
hg1941003
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363455
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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