A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999131



Internal ID17292083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:73619460..73632159hg38UCSC Ensembl
Outerchr15:73911801..73924500hg19UCSC Ensembl
Cytoband15q24.1
Allele length
AssemblyAllele length
hg3812700
hg1912700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951990
Supporting Variants
SamplesBILGI_BIOE
Known GenesNPTN
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999131
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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