A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337665



Internal ID20995218
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20904475..20931372hg38UCSC Ensembl
chr2:21104235..21131132hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3826898
hg1926898
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085006
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337665
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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