A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405225



Internal ID21062778
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88542301..88543900hg38UCSC Ensembl
chr5:87838119..87839718hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg381600
hg191600
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134835
Samples
Known GenesLINC00461
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405225
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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