A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6491530



Internal ID21149083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:96276987..96406030hg38UCSC Ensembl
chr13:96929241..97058284hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38129044
hg19129044
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015434
Samples
Known GenesHS6ST3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6491530
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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