A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5921



Internal ID15204093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:15185331..15213184hg38UCSC Ensembl
Outerchr10:15227330..15255183hg19UCSC Ensembl
Outerchr10:15267336..15295189hg18UCSC Ensembl
Outerchr10:15267336..15295189hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384894
hg194894
hg184894
hg174894
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3866
SamplesNA12878
Known GenesFAM171A1
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)nsv5921
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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