A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6398498



Internal ID21056051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120591257..120646069hg38UCSC Ensembl
chr5:119926952..119981764hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3854813
hg1954813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124700
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6398498
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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