A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10652



Internal ID15542146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:6358344..6387336hg38UCSC Ensembl
Outerchr9:6358344..6387336hg19UCSC Ensembl
Outerchr9:6348344..6377336hg18UCSC Ensembl
Outerchr9:6348344..6377336hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg388068
hg198068
hg188068
hg178068
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6468
Supporting Variants
SamplesNA18956
Known Genes
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)nssv10652
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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