A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1437



Internal ID15199314
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104701095..104733096hg38UCSC Ensembl
Outerchr14:105167432..105199433hg19UCSC Ensembl
Outerchr14:104238477..104270478hg18UCSC Ensembl
Outerchr14:104238477..104270478hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg388987
hg198987
hg188987
hg178987
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1220
SamplesNA19240
Known GenesADSSL1, INF2
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)nsv1437
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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