A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5910111



Internal ID22685321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:32646304..32650198hg38UCSC Ensembl
chr12:32799238..32803132hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg383895
hg193895
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17364872
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5910111
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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