A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335645



Internal ID20993198
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:205467833..205604926hg38UCSC Ensembl
chr2:206332557..206469650hg19UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg38137094
hg19137094
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18082913
Samples
Known GenesPARD3B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335645
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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