A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403595



Internal ID21061148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120413956..120467707hg38UCSC Ensembl
chr5:119749651..119803402hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg3853752
hg1953752
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126501
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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