A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17634688



Internal ID21826735
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:13494662..13494662hg38UCSC Ensembl
chr18:13494661..13494661hg19UCSC Ensembl
Cytoband18p11.21
Allele length
AssemblyAllele length
hg38154
hg19154
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6106608
Supporting Variants
Samples
Known GenesLDLRAD4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nssv17634688
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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