A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3838



Internal ID15201801
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:58352103..58386717hg38UCSC Ensembl
Outerchr3:58337830..58372444hg19UCSC Ensembl
Outerchr3:58312870..58347484hg18UCSC Ensembl
Outerchr3:58312870..58347484hg17UCSC Ensembl
Cytoband3p14.3
Allele length
AssemblyAllele length
hg386385
hg196385
hg186385
hg176385
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv303
SamplesNA19240
Known GenesPXK
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)nsv3838
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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