A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6403433



Internal ID21060986
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:45191788..45213431hg38UCSC Ensembl
chr5:45191890..45213533hg19UCSC Ensembl
Cytoband5p12
Allele length
AssemblyAllele length
hg3821644
hg1921644
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131594
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6403433
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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