A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6369553



Internal ID21027106
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158457585..158533292hg38UCSC Ensembl
chr3:158175374..158251081hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3875708
hg1975708
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094616
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6369553
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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