A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7593



Internal ID15552618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125094424..125125685hg38UCSC Ensembl
Outerchr10:126782993..126814254hg19UCSC Ensembl
Outerchr10:126772983..126804244hg18UCSC Ensembl
Outerchr10:126772983..126804244hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg388170
hg198170
hg188170
hg178170
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv6424
SamplesNA12156
Known GenesCTBP2
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)nsv7593
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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