A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6303



Internal ID15551199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:91465272..91510191hg38UCSC Ensembl
Outerchr8:92477500..92522419hg19UCSC Ensembl
Outerchr8:92546676..92591595hg18UCSC Ensembl
Outerchr8:92546676..92591595hg17UCSC Ensembl
Cytoband8q21.3
Allele length
AssemblyAllele length
hg3844920
hg1944920
hg1844920
hg1744920
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8525
SamplesNA12156
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)nsv6303
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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