A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5863749



Internal ID22638684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:3841804..3850870hg38UCSC Ensembl
chr12:3950970..3960036hg19UCSC Ensembl
Cytoband12p13.32
Allele length
AssemblyAllele length
hg389067
hg199067
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17461391
Samples
Known GenesPARP11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5863749
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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