A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366877



Internal ID22592546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:13243607..13243739hg38UCSC Ensembl
chr12:13396541..13396673hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38133
hg19133
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5910558
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366877
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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