A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6362594



Internal ID21020147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:182902801..182903900hg38UCSC Ensembl
chr3:182620589..182621688hg19UCSC Ensembl
Cytoband3q26.33
Allele length
AssemblyAllele length
hg381100
hg191100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18098466
Samples
Known GenesATP11B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6362594
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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