A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17518499



Internal ID21842858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:3475682..3475682hg38UCSC Ensembl
chr1:3392246..3392246hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6046321
Supporting Variants
Samples
Known GenesARHGEF16
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17518499
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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