A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925686



Internal ID22700913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:27062340..27062464hg38UCSC Ensembl
chr12:27215273..27215397hg19UCSC Ensembl
Cytoband12p11.23
Allele length
AssemblyAllele length
hg38125
hg19125
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358976
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925686
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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