A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487213



Internal ID21144766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:31144229..31144814hg38UCSC Ensembl
chr13:31718366..31718951hg19UCSC Ensembl
Cytoband13q12.3
Allele length
AssemblyAllele length
hg38586
hg19586
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007928
Samples
Known GenesHSPH1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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