A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10979



Internal ID15539567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:72853696..72882914hg38UCSC Ensembl
Outerchr17:70849835..70879053hg19UCSC Ensembl
Outerchr17:68361430..68390648hg18UCSC Ensembl
Outerchr17:68361430..68390648hg17UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg388832
hg198832
hg188832
hg178832
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2137
Supporting Variants
SamplesNA15510
Known GenesSLC39A11
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)nssv10979
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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