A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6376321



Internal ID21033874
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:17264628..17272471hg38UCSC Ensembl
chr5:17264737..17272580hg19UCSC Ensembl
Cytoband5p15.1
Allele length
AssemblyAllele length
hg387844
hg197844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18130233
Samples
Known GenesBASP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6376321
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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