A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952020



Internal ID16954207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:87880170..87886369hg38UCSC Ensembl
Outerchr15:88423401..88429600hg19UCSC Ensembl
Cytoband15q25.3
Allele length
AssemblyAllele length
hg386200
hg196200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2999164
SamplesBILGI_BIOE
Known GenesNTRK3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952020
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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