A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7542



Internal ID15552562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:108370102..108404274hg38UCSC Ensembl
Outerchr10:110129860..110164032hg19UCSC Ensembl
Outerchr10:110119850..110154022hg18UCSC Ensembl
Outerchr10:110119850..110154022hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg385262
hg195262
hg185262
hg175262
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8842
SamplesNA12156
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)nsv7542
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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