A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18005952



Internal ID20572992
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:103042201..103044700hg38UCSC Ensembl
chr13:103694551..103697050hg19UCSC Ensembl
Cytoband13q33.1
Allele length
AssemblyAllele length
hg382500
hg192500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6495025
Supporting Variants
Samples
Known GenesSLC10A2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18005952
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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