A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772512



Internal ID19306883
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:45027201..45032202hg38UCSC Ensembl
chr15:45319399..45324400hg19UCSC Ensembl
Cytoband15q21.1
Allele length
AssemblyAllele length
hg385002
hg195002
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075903
Supporting Variants
SamplesKWP1
Known GenesSORD
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772512
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