A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv8923



Internal ID15188255
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 StatusS
Merged Variantsnsv357
Supporting Variants
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)nssv8923
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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