A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862897



Internal ID22637832
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:102197631..102198830hg38UCSC Ensembl
chr12:102591409..102592608hg19UCSC Ensembl
Cytoband12q23.2
Allele length
AssemblyAllele length
hg381200
hg191200
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463882, nssv17465390
Samples
Known GenesPMCH
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862897
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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