A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6475222



Internal ID21132775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:94474497..94475601hg38UCSC Ensembl
chr11:94207663..94208767hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381105
hg191105
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995515
Samples
Known GenesMRE11A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6475222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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