A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17357363



Internal ID22583032
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:18025858..18029032hg38UCSC Ensembl
chr12:18178792..18181966hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg383175
hg193175
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5918869
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17357363
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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