A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1685



Internal ID15546248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:98497179..98531168hg38UCSC Ensembl
Outerchr15:99040408..99074397hg19UCSC Ensembl
Outerchr15:96857931..96891920hg18UCSC Ensembl
Outerchr15:96857931..96891920hg17UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg387011
hg197011
hg187011
hg177011
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1278
SamplesNA19240
Known GenesFAM169B
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)nsv1685
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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