A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9442



Internal ID15540393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:18874903..18910204hg38UCSC Ensembl
Outerchr10:19163832..19199133hg19UCSC Ensembl
Outerchr10:19203838..19239139hg18UCSC Ensembl
Outerchr10:19203838..19239139hg17UCSC Ensembl
Cytoband10p12.31
Allele length
AssemblyAllele length
hg3835302
hg1935302
hg1835302
hg1735302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv5999
Supporting Variants
SamplesNA18517
Known Genes
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)nssv9442
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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