A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18015574



Internal ID20582614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96013973..97010882hg38UCSC Ensembl
chr13:96666227..97663136hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38996910
hg19996910
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6488448
Supporting Variants
Samples
Known GenesHS6ST3, LINC00359, OXGR1, UGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18015574
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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