A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236047



Internal ID20803087
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:136185619..136214859hg38UCSC Ensembl
chr9:139077465..139106705hg19UCSC Ensembl
Cytoband9q34.3
Allele length
AssemblyAllele length
hg3829241
hg1929241
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6448268
Supporting Variants
Samples
Known GenesLHX3, QSOX2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236047
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00015


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