A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6406681



Internal ID21064234
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:80952710..80957640hg38UCSC Ensembl
chr5:80248529..80253459hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg384931
hg194931
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134126
Samples
Known GenesLOC102524628
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6406681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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