A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17368416



Internal ID22594085
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112541570..112541853hg38UCSC Ensembl
chr12:112979374..112979657hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38284
hg19284
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5939087
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17368416
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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