A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6487949



Internal ID21145502
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:108099300..108099714hg38UCSC Ensembl
chr13:108751648..108752062hg19UCSC Ensembl
Cytoband13q33.3
Allele length
AssemblyAllele length
hg38415
hg19415
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18007279
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6487949
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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