A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv585642



Internal ID15813638
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:15415547..15420686hg38UCSC Ensembl
chr12:15568481..15573620hg19UCSC Ensembl
chr12:15459748..15464887hg18UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg385140
hg195140
hg185140
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv498781
Supporting Variants
Samples
Known GenesPTPRO
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)nssv585642
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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