A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461861



Internal ID21119414
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:95924072..95926682hg38UCSC Ensembl
chr11:95657236..95659846hg19UCSC Ensembl
Cytoband11q21
Allele length
AssemblyAllele length
hg382611
hg192611
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17995427
Samples
Known GenesMTMR2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461861
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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