A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363095



Internal ID21020648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:99679352..99680146hg38UCSC Ensembl
chr3:99398196..99398990hg19UCSC Ensembl
Cytoband3q12.1
Allele length
AssemblyAllele length
hg38795
hg19795
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18105055
Samples
Known GenesCOL8A1, MIR548G
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363095
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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