A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952494



Internal ID16954681
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:121244498..121248497hg38UCSC Ensembl
Outerchr12:121682301..121686300hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg384000
hg194000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997367
SamplesBILGI_BIOE
Known GenesCAMKK2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952494
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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