A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4235



Internal ID15548924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:11051959..11077560hg38UCSC Ensembl
Outerchr4:11053583..11079184hg19UCSC Ensembl
Outerchr4:10662681..10688282hg18UCSC Ensembl
Outerchr4:10729852..10755453hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3814422
hg1914422
hg1814422
hg1714422
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2451
SamplesNA18555
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)nsv4235
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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