A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6043



Internal ID15550913
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:23334535..23368321hg38UCSC Ensembl
Outerchr10:23623464..23657250hg19UCSC Ensembl
Outerchr10:23663470..23697256hg18UCSC Ensembl
Outerchr10:23663470..23697256hg17UCSC Ensembl
Cytoband10p12.2
Allele length
AssemblyAllele length
hg385652
hg195652
hg185652
hg175652
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8489
SamplesNA12156
Known GenesC10orf67
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)nsv6043
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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