A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5909488



Internal ID22684698
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32017681..32018008hg38UCSC Ensembl
chr12:32170615..32170942hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38328
hg19328
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369093
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5909488
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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