A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6485032



Internal ID21142585
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:36871210..36881419hg38UCSC Ensembl
chr13:37445347..37455556hg19UCSC Ensembl
Cytoband13q13.3
Allele length
AssemblyAllele length
hg3810210
hg1910210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18008390
Samples
Known GenesSMAD9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6485032
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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