A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5763



Internal ID15196962
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:109642041..109657347hg38UCSC Ensembl
Outerchr1:110184663..110199969hg19UCSC Ensembl
Outerchr1:109986186..110001492hg18UCSC Ensembl
Outerchr1:109896705..109912011hg17UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3815307
hg1915307
hg1815307
hg1715307
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv2299
Supporting Variants
SamplesNA19129
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)nssv5763
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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