A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6488448



Internal ID21146001
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 StatusM
Merged Variants
Supporting Variantsnssv18015574
Samples
Known GenesHS6ST3, LINC00359, OXGR1, UGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6488448
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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