A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404402



Internal ID21061955
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:146116878..146119665hg38UCSC Ensembl
chr5:145496441..145499228hg19UCSC Ensembl
Cytoband5q32
Allele length
AssemblyAllele length
hg382788
hg192788
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126036
Samples
Known GenesLARS
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404402
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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