A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6354252



Internal ID21011805
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:139291208..139321910hg38UCSC Ensembl
chr2:140048778..140079480hg19UCSC Ensembl
Cytoband2q22.1
Allele length
AssemblyAllele length
hg3830703
hg1930703
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18077388
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6354252
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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