A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6480269



Internal ID21137822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:113199106..113199423hg38UCSC Ensembl
chr13:113853420..113853737hg19UCSC Ensembl
Cytoband13q34
Allele length
AssemblyAllele length
hg38318
hg19318
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007322
Samples
Known GenesPCID2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6480269
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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