A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8187



Internal ID15535677
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:167674906..167720015hg38UCSC Ensembl
Outerchr5:167101911..167147020hg19UCSC Ensembl
Outerchr5:167034489..167079598hg18UCSC Ensembl
Outerchr5:167034489..167079598hg17UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg3845110
hg1945110
hg1845110
hg1745110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5115
Supporting Variants
SamplesNA12156
Known GenesTENM2
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)nssv8187
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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