A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6105950



Internal ID22015183
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:56149062..56149062hg38UCSC Ensembl
chr19:56660431..56660431hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3879
hg1979
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17624070
Samples
Known GenesZNF444
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6105950
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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