A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8612



Internal ID15535252
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr9:74647132..74691922hg38UCSC Ensembl
Outerchr9:77262048..77306838hg19UCSC Ensembl
Outerchr9:76451868..76496658hg18UCSC Ensembl
Outerchr9:74491602..74536392hg17UCSC Ensembl
Cytoband9q21.13
Allele length
AssemblyAllele length
hg3844791
hg1944791
hg1844791
hg1744791
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6567
Supporting Variants
SamplesNA12156
Known GenesRORB
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)nssv8612
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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