A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231443



Internal ID20798483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:65707701..65743600hg38UCSC Ensembl
chr9:42688621..42724520hg19UCSC Ensembl
Cytoband9p12
Allele length
AssemblyAllele length
hg3835900
hg1935900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6444434
Supporting Variants
Samples
Known GenesFOXD4L2, FOXD4L4
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231443
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00614


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