A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410697



Internal ID21068250
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:117678083..117788606hg38UCSC Ensembl
chr5:117013778..117124301hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38110524
hg19110524
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5908n223
Supporting Variantsnssv18122875
Samples
Known GenesLOC102467224
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410697
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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