A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1165



Internal ID15199042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:64997218..65041683hg38UCSC Ensembl
Outerchr1:65462901..65507366hg19UCSC Ensembl
Outerchr1:65235489..65279954hg18UCSC Ensembl
Outerchr1:65174922..65219387hg17UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg3844466
hg1944466
hg1844466
hg1744466
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4638
SamplesNA19129
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)nsv1165
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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