A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv11182



Internal ID15539397
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:32803685..32847939hg38UCSC Ensembl
Outerchr8:32661203..32705457hg19UCSC Ensembl
Outerchr8:32780745..32824999hg18UCSC Ensembl
Outerchr8:32780745..32824999hg17UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg3844255
hg1944255
hg1844255
hg1744255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv6144
Supporting Variants
SamplesNA15510
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)nssv11182
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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