A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6337258



Internal ID20994811
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:231670886..231672415hg38UCSC Ensembl
chr2:232535597..232537126hg19UCSC Ensembl
Cytoband2q37.1
Allele length
AssemblyAllele length
hg381530
hg191530
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18086597
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6337258
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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