A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5312



Internal ID15196658
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:103858406..103903693hg38UCSC Ensembl
Outerchr10:105618164..105663451hg19UCSC Ensembl
Outerchr10:105608154..105653441hg18UCSC Ensembl
Outerchr10:105608154..105653441hg17UCSC Ensembl
Cytoband10q24.33
Allele length
AssemblyAllele length
hg3845288
hg1945288
hg1845288
hg1745288
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7531
Supporting Variants
SamplesNA19129
Known GenesOBFC1
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)nssv5312
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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