A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6353828



Internal ID21011381
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:210554469..210608968hg38UCSC Ensembl
chr2:211419193..211473692hg19UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3854500
hg1954500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18085138
Samples
Known GenesCPS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6353828
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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