A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv357



Internal ID15201506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64284335..64308789hg38UCSC Ensembl
Outerchr11:64051807..64076261hg19UCSC Ensembl
Outerchr11:63808383..63832837hg18UCSC Ensembl
Outerchr11:63808383..63832837hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386688
hg196688
hg186688
hg176688
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8923
SamplesNA12156
Known GenesBAD, ESRRA, GPR137, KCNK4, TEX40
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)nsv357
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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