A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355756



Internal ID22581425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:25952638..25953717hg38UCSC Ensembl
chr12:26105571..26106650hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg381080
hg191080
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5917424
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355756
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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