A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475529



Internal ID21133082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:46398765..46402586hg38UCSC Ensembl
chr11:46420315..46424136hg19UCSC Ensembl
Cytoband11p11.2
Allele length
AssemblyAllele length
hg383822
hg193822
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17991768
Samples
Known GenesAMBRA1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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