A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353358



Internal ID21010911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:119699211..119699901hg38UCSC Ensembl
chr2:120456787..120457477hg19UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg38691
hg19691
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075889
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353358
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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