A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv466



Internal ID15549391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:36986417..37031050hg38UCSC Ensembl
Outerchr1:37452018..37496651hg19UCSC Ensembl
Outerchr1:37224605..37269238hg18UCSC Ensembl
Outerchr1:37121111..37165744hg17UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg3844634
hg1944634
hg1844634
hg1744634
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv9013
SamplesNA12156
Known GenesGRIK3
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)nsv466
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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