A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6373580



Internal ID21031133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107226515..107228872hg38UCSC Ensembl
chr3:106945362..106947719hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg382358
hg192358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092672
Samples
Known GenesLINC00882
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6373580
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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