A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2999164



Internal ID16945430
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 StatusS
Merged Variantsnsv952020
Supporting Variants
SamplesBILGI_BIOE
Known GenesNTRK3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2999164
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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