A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763205



Internal ID19310532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:20432046..20441247hg38UCSC Ensembl
chr15:20637299..20646500hg19UCSC Ensembl
Cytoband15q11.1
Allele length
AssemblyAllele length
hg389202
hg199202
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075467
Supporting Variants
SamplesKWP1
Known GenesHERC2P3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763205
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