A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489676



Internal ID21147229
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 StatusM
Merged Variants
Supporting Variantsnssv18008091
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)nsv6489676
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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