A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6108134



Internal ID22017368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7518577..7518577hg38UCSC Ensembl
chr19:7583463..7583463hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17631071
Samples
Known GenesZNF358
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6108134
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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