A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856087



Internal ID22631022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:1710307..1716073hg38UCSC Ensembl
chr12:1819473..1825239hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg385767
hg195767
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17454841
Samples
Known GenesADIPOR2
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856087
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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