A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6454



Internal ID15551365
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:37860236..37895235hg38UCSC Ensembl
Outerchr10:38149164..38184163hg19UCSC Ensembl
Outerchr10:38189170..38224169hg18UCSC Ensembl
Outerchr10:38189170..38224169hg17UCSC Ensembl
Cytoband10p11.1
Allele length
AssemblyAllele length
hg385978
hg195978
hg185978
hg175978
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv846
SamplesNA19240
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)nsv6454
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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