A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv585671



Internal ID15467194
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr13:46465393..46467633hg38UCSC Ensembl
chr13:47039528..47041768hg19UCSC Ensembl
chr13:45937529..45939769hg18UCSC Ensembl
Cytoband13q14.13
Allele length
AssemblyAllele length
hg382241
hg192241
hg182241
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv498810
Supporting Variants
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)nssv585671
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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