A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1546



Internal ID15546109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:57263756..57297412hg38UCSC Ensembl
Outerchr15:57555954..57589610hg19UCSC Ensembl
Outerchr15:55343246..55376902hg18UCSC Ensembl
Outerchr15:55343246..55376902hg17UCSC Ensembl
Cytoband15q21.3
Allele length
AssemblyAllele length
hg387309
hg197309
hg187309
hg177309
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1254
SamplesNA19240
Known GenesTCF12
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)nsv1546
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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