A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5317



Internal ID15543337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:109803657..109821358hg38UCSC Ensembl
Outerchr10:111563415..111581116hg19UCSC Ensembl
Outerchr10:111553405..111571106hg18UCSC Ensembl
Outerchr10:111553405..111571106hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3817702
hg1917702
hg1817702
hg1717702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7545
Supporting Variants
SamplesNA19129
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)nssv5317
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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