A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5817



Internal ID15550664
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:82790370..82835105hg38UCSC Ensembl
Outerchr7:82419686..82464421hg19UCSC Ensembl
Outerchr7:82257622..82302357hg18UCSC Ensembl
Outerchr7:82064337..82109072hg17UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3844736
hg1944736
hg1844736
hg1744736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8391
SamplesNA12156
Known GenesPCLO
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)nsv5817
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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