A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17352497



Internal ID22578166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:54747963..54748172hg38UCSC Ensembl
chr12:55141747..55141956hg19UCSC Ensembl
Cytoband12q13.2
Allele length
AssemblyAllele length
hg38210
hg19210
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5943005
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17352497
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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