A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412998



Internal ID21070551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:115009298..115072439hg38UCSC Ensembl
chr5:114344995..114408136hg19UCSC Ensembl
Cytoband5q22.3
Allele length
AssemblyAllele length
hg3863142
hg1963142
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122826
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412998
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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