A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9326



Internal ID15193591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:41923301..41936877hg38UCSC Ensembl
Outerchr17:40079554..40093130hg19UCSC Ensembl
Outerchr17:37333080..37346656hg18UCSC Ensembl
Outerchr17:37333080..37346656hg17UCSC Ensembl
Cytoband17q21.2
Allele length
AssemblyAllele length
hg3812829
hg1912829
hg1812829
hg1712829
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2056
Supporting Variants
SamplesNA18517
Known GenesTTC25
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)nssv9326
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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