A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5862773



Internal ID22637708
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:104693611..104700970hg38UCSC Ensembl
chr12:105087389..105094748hg19UCSC Ensembl
Cytoband12q23.3
Allele length
AssemblyAllele length
hg387360
hg197360
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17463534
Samples
Known GenesCHST11
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5862773
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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