A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2997379



Internal ID17290331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:128968956..128976255hg38UCSC Ensembl
Outerchr12:129453501..129460800hg19UCSC Ensembl
Cytoband12q24.33
Allele length
AssemblyAllele length
hg387300
hg197300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952505
Supporting Variants
SamplesBILGI_BIOE
Known GenesGLT1D1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2997379
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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