A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354779



Internal ID21012332
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:154866901..154874600hg38UCSC Ensembl
chr2:155723413..155731112hg19UCSC Ensembl
Cytoband2q24.1
Allele length
AssemblyAllele length
hg387700
hg197700
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18078493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354779
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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