A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6097



Internal ID15204286
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:17404655..17432138hg38UCSC Ensembl
Outerchr8:17262164..17289647hg19UCSC Ensembl
Outerchr8:17306535..17334018hg18UCSC Ensembl
Outerchr8:17306535..17334018hg17UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg3811802
hg1911802
hg1811802
hg1711802
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5063
SamplesNA19129
Known GenesMTMR7
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)nsv6097
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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