A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6465529



Internal ID21123082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:85742942..85884995hg38UCSC Ensembl
chr11:85453985..85596038hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38142054
hg19142054
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994802
Samples
Known GenesCCDC83, SYTL2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6465529
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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