A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5188



Internal ID15544119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:6959788..6991596hg38UCSC Ensembl
Outerchr10:7001750..7033558hg19UCSC Ensembl
Outerchr10:7041756..7073564hg18UCSC Ensembl
Outerchr10:7041756..7073564hg17UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387456
hg197456
hg187456
hg177456
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5720
Supporting Variants
SamplesNA19129
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)nssv5188
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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