A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998051



Internal ID16944317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:114043342..114045341hg38UCSC Ensembl
Outerchr10:115803101..115805100hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv951851
Supporting Variants
SamplesBILGI_BIOE
Known GenesADRB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998051
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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