A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11180



Internal ID15539399
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:7768047..7785721hg38UCSC Ensembl
Outerchr8:7625569..7643243hg19UCSC Ensembl
Outerchr8:7662979..7680653hg18UCSC Ensembl
Outerchr8:7662979..7680653hg17UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg3820325
hg1920325
hg1820325
hg1720325
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6069
Supporting Variants
SamplesNA15510
Known GenesFAM90A10P, PRR23D1, PRR23D2
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)nssv11180
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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