A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6401412



Internal ID21058965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:116650002..116968427hg38UCSC Ensembl
chr5:115985698..116304123hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38318426
hg19318426
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18212479
Samples
Known GenesLOC102467223
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6401412
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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