A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5911



Internal ID15550768
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:113770502..113806788hg38UCSC Ensembl
Outerchr7:113410557..113446843hg19UCSC Ensembl
Outerchr7:113197793..113234079hg18UCSC Ensembl
Outerchr7:113004508..113040794hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3836287
hg1936287
hg1836287
hg1736287
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv678, nssv1682, nssv3569, nssv5018, nssv10576
SamplesNA12878, NA18956, NA18555, NA19240, NA19129
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)nsv5911
Frequency
Sample Size9
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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