A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1880



Internal ID15546443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:75363943..75393228hg38UCSC Ensembl
Outerchr16:75397841..75427126hg19UCSC Ensembl
Outerchr16:73955342..73984627hg18UCSC Ensembl
Outerchr16:73955342..73984627hg17UCSC Ensembl
Cytoband16q23.1
Allele length
AssemblyAllele length
hg3810220
hg1910220
hg1810220
hg1710220
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv10102
SamplesNA18956
Known GenesCFDP1
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)nsv1880
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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