A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488691



Internal ID21146244
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:102738401..102741300hg38UCSC Ensembl
chr13:103390751..103393650hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382900
hg192900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1985n223
Supporting Variantsnssv18005933
Samples
Known GenesCCDC168
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488691
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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