A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339775



Internal ID20997328
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:207681201..207681800hg38UCSC Ensembl
chr2:208545925..208546524hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38600
hg19600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082603
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339775
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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