A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11079



Internal ID15539629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:18267..49754hg38UCSC Ensembl
Outerchr4:18267..49648hg19UCSC Ensembl
Outerchr4:8267..39648hg18UCSC Ensembl
Outerchr4:8267..39648hg17UCSC Ensembl
Cytoband4p16.3
Allele length
AssemblyAllele length
hg388508
hg198508
hg188508
hg178508
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4192
Supporting Variants
SamplesNA15510
Known Genes
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv11079
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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