A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5858955



Internal ID22633890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3823352..3827819hg38UCSC Ensembl
chr12:3932518..3936985hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg384468
hg194468
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454039
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5858955
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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