A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6481981



Internal ID21139534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:99504524..99515799hg38UCSC Ensembl
chr13:100156778..100168053hg19UCSC Ensembl
Cytoband13q32.3
Allele length
AssemblyAllele length
hg3811276
hg1911276
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18016419
Samples
Known GenesTM9SF2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6481981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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