A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5686



Internal ID15550520
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:31273563..31287577hg38UCSC Ensembl
Outerchr7:31313177..31327191hg19UCSC Ensembl
Outerchr7:31279702..31293716hg18UCSC Ensembl
Outerchr7:31086417..31100431hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3814015
hg1914015
hg1814015
hg1714015
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3516
SamplesNA12878
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)nsv5686
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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