A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5851



Internal ID15204016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:95308446..95339854hg38UCSC Ensembl
Outerchr7:94937758..94969166hg19UCSC Ensembl
Outerchr7:94775694..94807102hg18UCSC Ensembl
Outerchr7:94582409..94613817hg17UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3831409
hg1931409
hg1831409
hg1731409
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8403
SamplesNA12156
Known GenesPON1
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)nsv5851
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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