A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6340669



Internal ID20998222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:16422399..16428123hg38UCSC Ensembl
chr2:16603667..16609391hg19UCSC Ensembl
Cytoband2p24.3
Allele length
AssemblyAllele length
hg385725
hg195725
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18079651
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6340669
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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