A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4844



Internal ID15202908
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:58476094..58509159hg38UCSC Ensembl
Outerchr5:57771921..57804986hg19UCSC Ensembl
Outerchr5:57807678..57840743hg18UCSC Ensembl
Outerchr5:57807678..57840743hg17UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg386374
hg196374
hg186374
hg176374
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8108
SamplesNA12156
Known GenesGAPT
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)nsv4844
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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