A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474677



Internal ID21132230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95770001..95770900hg38UCSC Ensembl
chr11:95503165..95504064hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995597
Samples
Known GenesFAM76B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474677
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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