A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv5166



Internal ID15542890
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:87899985..87922541hg38UCSC Ensembl
Outerchr9:90514900..90537456hg19UCSC Ensembl
Outerchr9:89704720..89727276hg18UCSC Ensembl
Outerchr9:87744454..87767010hg17UCSC Ensembl
Cytoband9q22.1
Allele length
AssemblyAllele length
hg3822557
hg1922557
hg1822557
hg1722557
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600
Supporting Variants
SamplesNA19129
Known GenesSPATA31C1
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)nssv5166
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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