A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18008091



Internal ID20575132
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:22913568..24325819hg38UCSC Ensembl
chr13:23487707..24899957hg19UCSC Ensembl
Cytoband13q12.12
Allele length
AssemblyAllele length
hg381412252
hg191412251
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6489676
Supporting Variants
Samples
Known GenesANKRD20A19P, C1QTNF9, C1QTNF9B, C1QTNF9B-AS1, LINC00327, MIPEP, MIR2276, SACS, SACS-AS1, SGCG, SPATA13, SPATA13-AS1, TNFRSF19
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18008091
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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