A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5920136



Internal ID22695359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6766515..6766725hg38UCSC Ensembl
chr12:6875681..6875891hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38211
hg19211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17354695
Samples
Known GenesPTMS
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5920136
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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