A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6474790



Internal ID21132343
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95856501..95857800hg38UCSC Ensembl
chr11:95589665..95590964hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg381300
hg191300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995602
Samples
Known GenesMTMR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6474790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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