A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv966



Internal ID15198114
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:112340440..112365512hg38UCSC Ensembl
Outerchr10:114100198..114125270hg19UCSC Ensembl
Outerchr10:114090188..114115260hg18UCSC Ensembl
Outerchr10:114090188..114115260hg17UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg3825073
hg1925073
hg1825073
hg1725073
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7552
Supporting Variants
SamplesNA19240
Known GenesGUCY2GP
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)nssv966
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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