A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6342091



Internal ID20999644
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:109516520..109516775hg38UCSC Ensembl
chr2:110274097..110274352hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075357
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6342091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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