A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5913342



Internal ID22688558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29145710..29145927hg38UCSC Ensembl
chr12:29298643..29298860hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38218
hg19218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17355175
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5913342
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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