A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6463226



Internal ID21120779
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:83899032..83899295hg38UCSC Ensembl
chr11:83610075..83610338hg19UCSC Ensembl
Cytoband11q14.1
Allele length
AssemblyAllele length
hg38264
hg19264
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17994402
Samples
Known GenesDLG2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6463226
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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