A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6366256



Internal ID21023809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159009226..159161043hg38UCSC Ensembl
chr3:158727015..158878832hg19UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg38151818
hg19151818
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094660
Samples
Known GenesIQCJ, IQCJ-SCHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6366256
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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