A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409332



Internal ID21066885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:129109272..129140014hg38UCSC Ensembl
chr5:128444965..128475707hg19UCSC Ensembl
Cytoband5q23.3
Allele length
AssemblyAllele length
hg3830743
hg1930743
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124454
Samples
Known GenesISOC1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409332
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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