A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3763350



Internal ID19306635
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46557217..46602718hg38UCSC Ensembl
chr10:46946899..46992400hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg3845502
hg1945502
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1075818
Supporting Variants
SamplesKWP1
Known GenesSYT15
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3763350
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