A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5831



Internal ID15203994
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:12862255..12897166hg38UCSC Ensembl
Outerchr10:12904255..12939166hg19UCSC Ensembl
Outerchr10:12944261..12979172hg18UCSC Ensembl
Outerchr10:12944261..12979172hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg386070
hg196070
hg186070
hg176070
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv740
SamplesNA19240
Known GenesCCDC3
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)nsv5831
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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