A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372474



Internal ID21030027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158368114..158368597hg38UCSC Ensembl
chr3:158085903..158086386hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38484
hg19484
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094035
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372474
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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