A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv952409



Internal ID16954596
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:9914804..9963203hg38UCSC Ensembl
Outerchr18:9914801..9963200hg19UCSC Ensembl
Cytoband18p11.22
Allele length
AssemblyAllele length
hg3848400
hg1948400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998842
SamplesBILGI_BIOE
Known GenesVAPA
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv952409
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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