A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337625



Internal ID20995178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:223851924..223859966hg38UCSC Ensembl
chr2:224716641..224724683hg19UCSC Ensembl
Cytoband2q36.1
Allele length
AssemblyAllele length
hg388043
hg198043
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18083736
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337625
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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