A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952718



Internal ID16954905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:144334870..144389049hg38UCSC Ensembl
Outerchr1:148628601..148682800hg19UCSC Ensembl
Cytoband1q21.2
Allele length
AssemblyAllele length
hg3854180
hg1954200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2997290
SamplesBILGI_BIOE
Known GenesLOC101929780
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952718
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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