A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17460233



Internal ID22518119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3830620..3841803hg38UCSC Ensembl
chr12:3939786..3950969hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg3811184
hg1911184
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5855306
Supporting Variants
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17460233
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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