A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395018



Internal ID21052571
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:32327727..32344700hg38UCSC Ensembl
chr5:32327833..32344806hg19UCSC Ensembl
Cytoband5p13.3
Allele length
AssemblyAllele length
hg3816974
hg1916974
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130922
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395018
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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