A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6473850



Internal ID21131403
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61604391..61604959hg38UCSC Ensembl
chr11:61371863..61372431hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg38569
hg19569
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993151
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6473850
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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