A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6372903



Internal ID21030456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:121922572..121942534hg38UCSC Ensembl
chr3:121641419..121661381hg19UCSC Ensembl
Cytoband3q13.33
Allele length
AssemblyAllele length
hg3819963
hg1919963
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18095184
Samples
Known GenesSLC15A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6372903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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