A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17626103



Internal ID21818150
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:7471973..7471973hg38UCSC Ensembl
chr19:7536859..7536859hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106636
Supporting Variants
Samples
Known GenesARHGEF18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17626103
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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