A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7511



Internal ID15552528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:98496224..98534170hg38UCSC Ensembl
Outerchr10:100255981..100293927hg19UCSC Ensembl
Outerchr10:100245971..100283917hg18UCSC Ensembl
Outerchr10:100245971..100283917hg17UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg3837947
hg1937947
hg1837947
hg1737947
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8833
SamplesNA12156
Known GenesHPSE2
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)nsv7511
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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