A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8455



Internal ID15188723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:14658226..14693079hg38UCSC Ensembl
Outerchr10:14700225..14735078hg19UCSC Ensembl
Outerchr10:14740231..14775084hg18UCSC Ensembl
Outerchr10:14740231..14775084hg17UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg3834854
hg1934854
hg1834854
hg1734854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5888
Supporting Variants
SamplesNA12156
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)nssv8455
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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