A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6458120



Internal ID21115673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:65040220..65093556hg38UCSC Ensembl
chr11:64807692..64861028hg19UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg3853337
hg1953337
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994085
Samples
Known GenesARL2-SNX15, CDCA5, NAALADL1, SAC3D1, SNX15, TMEM262, ZFPL1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6458120
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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