A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8602



Internal ID15535262
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:33132729..33149711hg38UCSC Ensembl
Outerchr9:33132727..33149709hg19UCSC Ensembl
Outerchr9:33122727..33139709hg18UCSC Ensembl
Outerchr9:33122727..33139709hg17UCSC Ensembl
Cytoband9p13.3
Allele length
AssemblyAllele length
hg3816983
hg1916983
hg1816983
hg1716983
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6523
Supporting Variants
SamplesNA12156
Known GenesB4GALT1
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)nssv8602
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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