A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5899



Internal ID15204068
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14803505..14837648hg38UCSC Ensembl
Outerchr10:14845504..14879647hg19UCSC Ensembl
Outerchr10:14885510..14919653hg18UCSC Ensembl
Outerchr10:14885510..14919653hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385288
hg195288
hg185288
hg175288
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8460
SamplesNA12156
Known GenesCDNF
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)nsv5899
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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