A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6371792



Internal ID21029345
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:158228101..158230700hg38UCSC Ensembl
chr3:157945890..157948489hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg382600
hg192600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18096831
Samples
Known GenesRSRC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6371792
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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