A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6364146



Internal ID21021699
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:109336107..109341597hg38UCSC Ensembl
chr3:109054954..109060444hg19UCSC Ensembl
Cytoband3q13.13
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18093377
Samples
Known GenesDPPA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6364146
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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