A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952786



Internal ID16954973
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:1696435..1707934hg38UCSC Ensembl
Outerchr12:1805601..1817100hg19UCSC Ensembl
Cytoband12p13.33
Allele length
AssemblyAllele length
hg3811500
hg1911500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999666
SamplesBILGI_BIOE
Known GenesADIPOR2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952786
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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