A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv499094



Internal ID15815190
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17769687..17859621hg38UCSC Ensembl
chr12:17922621..18012555hg19UCSC Ensembl
chr12:17813888..17903822hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3889935
hg1989935
hg1889935
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv15n47
Supporting Variantsnssv585500
Samples
Known Genes
MethodSequencing
AnalysisFor each individuals we constructed a whole genomic library of approximately 1 million clones using a fosdmid subcloning strategy Paried end sequences from each clone were sequenced and searched against NCBI build35. Individual fosmid clones corresponding to regions of structural difference relative to the genome reference were selected and sequenced. The breakpoints determined from complete fosmid sequencing are given using the NCBI build36 genome assembly.
PlatformCapillary
Comments
ReferenceKidd_et_al_2010b
Pubmed ID21111241
Accession Number(s)nsv499094
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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