A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6493903



Internal ID21151456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:98735313..98739818hg38UCSC Ensembl
chr13:99387567..99392072hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg384506
hg194506
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016379
Samples
Known GenesSLC15A1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6493903
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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