A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8664



Internal ID15188514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:46280158..46310106hg38UCSC Ensembl
Outerchr10:47651394..47681342hg19UCSC Ensembl
Outerchr10:47121400..47151348hg18UCSC Ensembl
Outerchr10:47121400..47151348hg17UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg385880
hg195880
hg185880
hg175880
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6543
Supporting Variants
SamplesNA12156
Known GenesANTXRL
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)nssv8664
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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