A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363844



Internal ID21021397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:107285782..107292168hg38UCSC Ensembl
chr3:107004629..107011015hg19UCSC Ensembl
Cytoband3q13.12
Allele length
AssemblyAllele length
hg386387
hg196387
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18092676
Samples
Known GenesLINC00883
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363844
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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