A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6349562



Internal ID21007115
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65659792..65660118hg38UCSC Ensembl
chr2:65886926..65887252hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg38327
hg19327
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089986
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6349562
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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