A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17631949



Internal ID21823996
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:41893350..41893534hg38UCSC Ensembl
chr19:42397421..42397605hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38185
hg19185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6047749
Supporting Variants
Samples
Known GenesARHGEF1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17631949
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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