A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9971



Internal ID15540067
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:82579258..82592595hg38UCSC Ensembl
Outerchr17:80537134..80550471hg19UCSC Ensembl
Outerchr17:78130423..78143760hg18UCSC Ensembl
Outerchr17:78130423..78143760hg17UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg386428
hg196428
hg186428
hg176428
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2167
Supporting Variants
SamplesNA18507
Known GenesFOXK2
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)nssv9971
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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