A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5926683



Internal ID22701910
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:14750678..14767271hg38UCSC Ensembl
chr12:14903612..14920205hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3816594
hg1916594
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17369472
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5926683
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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