A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6338988



Internal ID20996541
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139578362..139802781hg38UCSC Ensembl
chr2:140335931..140560350hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg38224420
hg19224420
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077422
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6338988
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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