A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6469880



Internal ID21127433
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:96206355..96234788hg38UCSC Ensembl
chr11:95939519..95967952hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg3828434
hg1928434
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995450
Samples
Known GenesMAML2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6469880
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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