A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7586



Internal ID15205924
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122982687..123016052hg38UCSC Ensembl
Outerchr10:124742203..124775568hg19UCSC Ensembl
Outerchr10:124732193..124765558hg18UCSC Ensembl
Outerchr10:124732193..124765558hg17UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386664
hg196664
hg186664
hg176664
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1913, nssv10783
SamplesNA18956, NA18555
Known GenesACADSB, IKZF5, PSTK
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)nsv7586
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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