A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997388



Internal ID16943654
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:132773415..132840614hg38UCSC Ensembl
Outerchr12:133350001..133417200hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg3867200
hg1967200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952513
Supporting Variants
SamplesBILGI_BIOE
Known GenesCHFR, GOLGA3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997388
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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