A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1734



Internal ID15541017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:46928739..46973244hg38UCSC Ensembl
Outerchr8:47840361..47884867hg19UCSC Ensembl
Outerchr8:47959526..48004032hg18UCSC Ensembl
Outerchr8:47959526..48004032hg17UCSC Ensembl
Cytoband8q11.1
Allele length
AssemblyAllele length
hg3844506
hg1944507
hg1844507
hg1744507
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6177
Supporting Variants
SamplesNA18555
Known Genes
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)nssv1734
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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