A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17455983



Internal ID22513860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:41100794..41110511hg38UCSC Ensembl
chr12:41494596..41504313hg19UCSC Ensembl
Cytoband12q12
Allele length
AssemblyAllele length
hg389718
hg199718
Variant TypeOTHER copy number variation
Copy Number0
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5864375
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17455983
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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