A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5929295



Internal ID22704546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112418262..112418527hg38UCSC Ensembl
chr12:112856066..112856331hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38266
hg19266
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17356247
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5929295
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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