A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6112499



Internal ID22021732
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:1368894..1368894hg38UCSC Ensembl
chr19:1368893..1368893hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38148
hg19148
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17637180
Samples
Known GenesMUM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6112499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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