A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv954461



Internal ID17303335
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:32396709..32428608hg38UCSC Ensembl
Outerchr3:32438201..32470100hg19UCSC Ensembl
Cytoband3p22.3
Allele length
AssemblyAllele length
hg3831900
hg1931900
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001357
SamplesBILGI_BIOE
Known GenesCMTM7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv954461
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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