A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17366387



Internal ID22592056
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:93900302..93902239hg38UCSC Ensembl
chr12:94294078..94296015hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg381938
hg191938
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5928450
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17366387
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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