A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461157



Internal ID21118710
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:67327118..67328073hg38UCSC Ensembl
chr11:67094589..67095544hg19UCSC Ensembl
Cytoband11q13.2
Allele length
AssemblyAllele length
hg38956
hg19956
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17993483
Samples
Known GenesLOC100130987
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461157
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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