A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6363181



Internal ID21020734
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160497424..160497909hg38UCSC Ensembl
chr3:160215212..160215697hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38486
hg19486
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094771
Samples
Known GenesKPNA4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6363181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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