A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7592



Internal ID15552617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:125079935..125103851hg38UCSC Ensembl
Outerchr10:126768504..126792420hg19UCSC Ensembl
Outerchr10:126758494..126782410hg18UCSC Ensembl
Outerchr10:126758494..126782410hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3823917
hg1923917
hg1823917
hg1723917
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8857
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)nsv7592
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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