A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6489698



Internal ID21147251
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:95954178..95954656hg38UCSC Ensembl
chr13:96606432..96606910hg19UCSC Ensembl
Cytoband13q32.1
Allele length
AssemblyAllele length
hg38479
hg19479
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18015423
Samples
Known GenesUGGT2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6489698
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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