A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6408443



Internal ID21065996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:87883411..87891556hg38UCSC Ensembl
chr5:87179228..87187373hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg388146
hg198146
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134767
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6408443
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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