A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5877



Internal ID15204044
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14521492..14555125hg38UCSC Ensembl
Outerchr10:14563491..14597124hg19UCSC Ensembl
Outerchr10:14603497..14637130hg18UCSC Ensembl
Outerchr10:14603497..14637130hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg385638
hg195638
hg185638
hg175638
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5203
SamplesNA19129
Known GenesFAM107B
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)nsv5877
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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