A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1741



Internal ID15199618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:15387639..15416844hg38UCSC Ensembl
Outerchr16:15481496..15510701hg19UCSC Ensembl
Outerchr16:15388997..15418202hg18UCSC Ensembl
Outerchr16:15388997..15418202hg17UCSC Ensembl
Cytoband16p13.11
Allele length
AssemblyAllele length
hg3810280
hg1910280
hg1810280
hg1710280
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10081
SamplesNA18956
Known GenesMPV17L
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)nsv1741
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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