A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999157



Internal ID17292109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82905149..82917548hg38UCSC Ensembl
Outerchr15:83573901..83586300hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3812400
hg1912400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952014
Supporting Variants
SamplesBILGI_BIOE
Known GenesHOMER2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999157
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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