A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1435



Internal ID15545998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr14:104483327..104505620hg38UCSC Ensembl
Outerchr14:104949664..104971957hg19UCSC Ensembl
Outerchr14:104020709..104043002hg18UCSC Ensembl
Outerchr14:104020709..104043002hg17UCSC Ensembl
Cytoband14q32.33
Allele length
AssemblyAllele length
hg386173
hg196173
hg186173
hg176173
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4132, nssv2087, nssv5526, nssv9245
SamplesNA12156, NA12878, NA18555, NA19129
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)nsv1435
Frequency
Sample Size9
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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