A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1641



Internal ID15546204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:82877686..82896678hg38UCSC Ensembl
Outerchr15:83546438..83565430hg19UCSC Ensembl
Outerchr15:81343492..81356434hg18UCSC Ensembl
Outerchr15:81343492..81356434hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg387683
hg197683
hg187683
hg177683
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1270, nssv6645
SamplesNA12156, NA19240
Known GenesHOMER2
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)nsv1641
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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