A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5865968



Internal ID22640903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:124438035..124440417hg38UCSC Ensembl
chr12:124922581..124924963hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg382383
hg192383
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17453969
Samples
Known GenesNCOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5865968
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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