A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355338



Internal ID21012891
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:113283830..113287056hg38UCSC Ensembl
chr2:114041407..114044633hg19UCSC Ensembl
Cytoband2q13
Allele length
AssemblyAllele length
hg383227
hg193227
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18075592
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355338
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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