A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4157



Internal ID15202152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:187094850..187129650hg38UCSC Ensembl
Outerchr3:186812638..186847438hg19UCSC Ensembl
Outerchr3:188295332..188330132hg18UCSC Ensembl
Outerchr3:188295340..188330140hg17UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg386195
hg196195
hg186195
hg176195
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv355
SamplesNA19240
Known GenesRPL39L
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)nsv4157
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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