A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6370513



Internal ID21028066
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158310487..158346468hg38UCSC Ensembl
chr3:158028276..158064257hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3835982
hg1935982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094033
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6370513
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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