A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5934815



Internal ID22710147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:57873746..57873844hg38UCSC Ensembl
chr12:58267529..58267627hg19UCSC Ensembl
Cytoband12q14.1
Allele length
AssemblyAllele length
hg3899
hg1999
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17366453
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5934815
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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