A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3001335



Internal ID16947601
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:13311201..13345400hg38UCSC Ensembl
Outerchr3:13352701..13386900hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg3834200
hg1934200
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv955315
Supporting Variants
SamplesBILGI_BIOE
Known GenesNUP210
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv3001335
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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