A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1270



Internal ID15544454
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
hg386304
hg196304
hg186304
hg176304
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv1641
Supporting Variants
SamplesNA19240
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)nssv1270
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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