A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3766800



Internal ID18965971
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:84207047..84213748hg38UCSC Ensembl
chr15:84875799..84882500hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg386702
hg196702
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1077809
Supporting Variants
SamplesKWP1
Known GenesLOC388152, LOC440300
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3766800
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer