A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6106636



Internal ID22015870
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 StatusM
Merged Variants
Supporting Variantsnssv17626103
Samples
Known GenesARHGEF18
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6106636
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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