A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11192



Internal ID15539387
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:85774384..85851337hg38UCSC Ensembl
Outerchr8:86801686..86863566hg19UCSC Ensembl
Outerchr8:86871247..86932655hg18UCSC Ensembl
Outerchr8:86871247..86932655hg17UCSC Ensembl
Cytoband8q21.2
Allele length
AssemblyAllele length
hg3876954
hg1961881
hg1861409
hg1761409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6285
Supporting Variants
SamplesNA15510
Known GenesREXO1L2P
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)nssv11192
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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