A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv955351



Internal ID16957538
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:136163759..136195858hg38UCSC Ensembl
Outerchr3:135882601..135914700hg19UCSC Ensembl
Cytoband3q22.3
Allele length
AssemblyAllele length
hg3832100
hg1932100
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001468
SamplesBILGI_BIOE
Known GenesMSL2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv955351
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