A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6380876



Internal ID21038429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:8868526..8871174hg38UCSC Ensembl
chr5:8868638..8871286hg19UCSC Ensembl
Cytoband5p15.31
Allele length
AssemblyAllele length
hg382649
hg192649
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134848
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6380876
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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