A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6456104



Internal ID21113657
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:93075319..93079213hg38UCSC Ensembl
chr11:92808485..92812379hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg383895
hg193895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17996443
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6456104
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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