A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv354



Internal ID15548159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr11:64044979..64079484hg38UCSC Ensembl
Outerchr11:63812451..63846956hg19UCSC Ensembl
Outerchr11:63569027..63603532hg18UCSC Ensembl
Outerchr11:63569027..63603532hg17UCSC Ensembl
Cytoband11q13.1
Allele length
AssemblyAllele length
hg386490
hg196490
hg186490
hg176490
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1014
SamplesNA19240
Known GenesMACROD1
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)nsv354
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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