A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7621



Internal ID15552649
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:131081871..131117163hg38UCSC Ensembl
Outerchr10:132880134..132915426hg19UCSC Ensembl
Outerchr10:132770124..132805416hg18UCSC Ensembl
Outerchr10:132770124..132805416hg17UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3835293
hg1935293
hg1835293
hg1735293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1915
SamplesNA18555
Known GenesTCERG1L
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)nsv7621
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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