A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv7269



Internal ID15552261
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:83050924..83078389hg38UCSC Ensembl
Outerchr15:83719676..83747141hg19UCSC Ensembl
Outerchr15:81510680..81538145hg18UCSC Ensembl
Outerchr15:81510680..81538145hg17UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3827466
hg1927466
hg1827466
hg1727466
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1271
SamplesNA19240
Known GenesBTBD1, MIR4515
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)nsv7269
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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