A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18212232



Internal ID20779272
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:188146421..188284686hg38UCSC Ensembl
chr3:187864209..188002474hg19UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg38138266
hg19138266
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6362238
Supporting Variants
Samples
Known GenesFLJ42393, LPP, LPP-AS2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18212232
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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