A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1680



Internal ID15546243
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:95737124..95767991hg38UCSC Ensembl
Outerchr15:96280353..96311220hg19UCSC Ensembl
Outerchr15:94081357..94112224hg18UCSC Ensembl
Outerchr15:94081357..94112224hg17UCSC Ensembl
Cytoband15q26.2
Allele length
AssemblyAllele length
hg388410
hg198410
hg188410
hg178410
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv5576
SamplesNA19129
Known Genes
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)nsv1680
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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