A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6461693



Internal ID21119246
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65028970..65030242hg38UCSC Ensembl
chr11:64796442..64797714hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg381273
hg191273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994083
Samples
Known GenesARL2-SNX15, SNX15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6461693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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