A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337299



Internal ID20994852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:19478956..19482639hg38UCSC Ensembl
chr2:19678717..19682400hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg383684
hg193684
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082230
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337299
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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