A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6451161



Internal ID21108714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:133430842..133431879hg38UCSC Ensembl
chr9:136295962..136297000hg19UCSC Ensembl
Cytoband9q34.2
Allele length
AssemblyAllele length
hg381038
hg191039
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18177110
Samples
Known GenesADAMTS13
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6451161
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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