A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv2026



Internal ID15199903
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:33015218..33060034hg38UCSC Ensembl
Outerchr17:31342236..31387052hg19UCSC Ensembl
Outerchr17:28366349..28411165hg18UCSC Ensembl
Outerchr17:28366349..28411165hg17UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3844817
hg1944817
hg1844817
hg1744817
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7322
SamplesNA12156
Known GenesASIC2
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)nsv2026
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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