A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851745



Internal ID22626680
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3873215..3877764hg38UCSC Ensembl
chr12:3982381..3986930hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg384550
hg194550
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463307
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5851745
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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