A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7553



Internal ID8519556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:113085948..113130887hg38UCSC Ensembl
Outerchr10:114845707..114890646hg19UCSC Ensembl
Outerchr10:114835697..114880636hg18UCSC Ensembl
Outerchr10:114835697..114880636hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3844940
hg1944940
hg1844940
hg1744940
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8846
SamplesNA12156
Known GenesTCF7L2
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)nsv7553
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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