A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6351587



Internal ID21009140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:20591334..20633384hg38UCSC Ensembl
chr2:20791094..20833144hg19UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3842051
hg1942051
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18208094
Samples
Known GenesHS1BP3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6351587
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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