A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9622



Internal ID15540181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:89441683..89471444hg38UCSC Ensembl
Outerchr3:89490833..89520594hg19UCSC Ensembl
Outerchr3:89573523..89603284hg18UCSC Ensembl
Outerchr3:89573523..89603284hg17UCSC Ensembl
Cytoband3p11.1
Allele length
AssemblyAllele length
hg3829762
hg1929762
hg1829762
hg1729762
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv3908
Supporting Variants
SamplesNA18507
Known GenesEPHA3
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)nssv9622
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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