A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17355947



Internal ID22581616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:65738473..65738636hg38UCSC Ensembl
chr12:66132253..66132416hg19UCSC Ensembl
Cytoband12q14.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944836
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17355947
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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