A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10184



Internal ID15195928
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109635606..109662341hg38UCSC Ensembl
Outerchr1:110178228..110204963hg19UCSC Ensembl
Outerchr1:109979751..110006486hg18UCSC Ensembl
Outerchr1:109890270..109917005hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3826736
hg1926736
hg1826736
hg1726736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv2299
Supporting Variants
SamplesNA18956
Known GenesGSTM4
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)nssv10184
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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