A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361564



Internal ID21019117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121898501..121899105hg38UCSC Ensembl
chr3:121617348..121617952hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg38605
hg19605
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095182
Samples
Known GenesSLC15A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361564
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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