A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355683



Internal ID21013236
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:169002018..169002262hg38UCSC Ensembl
chr3:168719806..168720050hg19UCSC Ensembl
Cytoband3q26.2
Allele length
AssemblyAllele length
hg38245
hg19245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18097433
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355683
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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