A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1114459



Internal ID19272179
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:184159027..184159615hg38UCSC Ensembl
Outerchr3:183876815..183877403hg19UCSC Ensembl
Cytoband3q27.1
Allele length
AssemblyAllele length
hg38589
hg19589
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3974358
SamplesKWS2
Known GenesDVL3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1114459
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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