A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008989



Internal ID20576031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36266950..36273175hg38UCSC Ensembl
chr13:36841087..36847312hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg386226
hg196226
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6483980
Supporting Variants
Samples
Known GenesCCDC169, CCDC169-SOHLH2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008989
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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