A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17521104



Internal ID21845463
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:17683228..17683423hg38UCSC Ensembl
chr1:18009723..18009918hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38196
hg19196
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5981855
Supporting Variants
Samples
Known GenesARHGEF10L
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17521104
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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