A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6411029



Internal ID21068582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117693608..118716266hg38UCSC Ensembl
chr5:117029303..118051961hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg381022659
hg191022659
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18122876
Samples
Known GenesLOC100505811, LOC101927280, LOC102467224, LOC102467225
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6411029
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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