A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6467222



Internal ID21124775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:131504916..131505358hg38UCSC Ensembl
chr11:131374810..131375252hg19UCSC Ensembl
Cytoband11q25
Allele length
AssemblyAllele length
hg38443
hg19443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17987912
Samples
Known GenesNTM
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6467222
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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