A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10647



Internal ID15195465
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:143611035..143634307hg38UCSC Ensembl
Outerchr8:144693205..144716477hg19UCSC Ensembl
Outerchr8:144764348..144787620hg18UCSC Ensembl
Outerchr8:144764348..144787620hg17UCSC Ensembl
Cytoband8q24.3
Allele length
AssemblyAllele length
hg3823273
hg1923273
hg1823273
hg1723273
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6439
Supporting Variants
SamplesNA18956
Known GenesTSTA3
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)nssv10647
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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