A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951979



Internal ID16954166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:66398363..66411762hg38UCSC Ensembl
Outerchr15:66690701..66704100hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3813400
hg1913400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999119
SamplesBILGI_BIOE
Known GenesMAP2K1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951979
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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