A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5861689



Internal ID22636624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1724658..1728957hg38UCSC Ensembl
chr12:1833824..1838123hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17464364
Samples
Known GenesADIPOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5861689
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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