A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411563



Internal ID21069116
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:74886501..74890000hg38UCSC Ensembl
chr5:74182326..74185825hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18132267
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411563
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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