A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17199657



Internal ID21647166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:59298594..59298594hg38UCSC Ensembl
chr18:56965826..56965826hg19UCSC Ensembl
Cytoband18q21.32
Allele length
AssemblyAllele length
hg38279
hg19279
Variant TypeCNV alu insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5703549
Supporting Variants
Samples
Known GenesCPLX4
MethodSequencing
AnalysisMobile Element Locator Tool (MELT)
Platform
CommentsInsertion of a Alu mobile element relative to the reference
ReferenceChuang_et_al_2021
Pubmed ID34772701
Accession Number(s)nssv17199657
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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