A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7566



Internal ID15552588
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:118017102..118062319hg38UCSC Ensembl
Outerchr10:119776613..119821830hg19UCSC Ensembl
Outerchr10:119766603..119811820hg18UCSC Ensembl
Outerchr10:119766603..119811820hg17UCSC Ensembl
Cytoband10q26.11
Allele length
AssemblyAllele length
hg3845218
hg1945218
hg1845218
hg1745218
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8851
SamplesNA12156
Known GenesCASC2, RAB11FIP2
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)nsv7566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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