A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7308



Internal ID15536556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:9463447..9496976hg38UCSC Ensembl
Outerchr17:9366764..9400293hg19UCSC Ensembl
Outerchr17:9307489..9341018hg18UCSC Ensembl
Outerchr17:9307489..9341018hg17UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg385902
hg195902
hg185902
hg175902
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1973
Supporting Variants
SamplesNA12156
Known GenesSTX8
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)nssv7308
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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