A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv6289



Internal ID15537574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:8779567..8811841hg38UCSC Ensembl
Outerchr10:8821530..8853804hg19UCSC Ensembl
Outerchr10:8861536..8893810hg18UCSC Ensembl
Outerchr10:8861536..8893810hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387163
hg197163
hg187163
hg177163
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5765
Supporting Variants
SamplesNA12156
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)nssv6289
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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