A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5168



Internal ID15542886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:88259716..88271363hg38UCSC Ensembl
Outerchr9:90874631..90886278hg19UCSC Ensembl
Outerchr9:90064451..90076098hg18UCSC Ensembl
Outerchr9:88104185..88115832hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3811648
hg1911648
hg1811648
hg1711648
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604
Supporting Variants
SamplesNA19129
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)nssv5168
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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