A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442068



Internal ID21099621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:13713601..13714500hg38UCSC Ensembl
chr11:13735148..13736047hg19UCSC Ensembl
Cytoband11p15.2
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17989192
Samples
Known GenesFAR1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442068
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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