A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5090



Internal ID15549865
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:157750462..157785442hg38UCSC Ensembl
Outerchr5:157177470..157212450hg19UCSC Ensembl
Outerchr5:157110048..157145028hg18UCSC Ensembl
Outerchr5:157110048..157145028hg17UCSC Ensembl
Cytoband5q33.3
Allele length
AssemblyAllele length
hg386184
hg196184
hg186184
hg176184
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4873, nssv8176
SamplesNA12156, NA19129
Known GenesLSM11
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)nsv5090
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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