A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6409115



Internal ID21066668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116255201..116258300hg38UCSC Ensembl
chr5:115590898..115593997hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg383100
hg193100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5907n223
Supporting Variantsnssv18125700
Samples
Known GenesCOMMD10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6409115
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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