A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv498969



Internal ID15815065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr20:34228122..34231430hg38UCSC Ensembl
chr20:32815928..32819236hg19UCSC Ensembl
chr20:32279589..32282897hg18UCSC Ensembl
Cytoband20q11.22
Allele length
AssemblyAllele length
hg383309
hg193309
hg183309
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv585830
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)nsv498969
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer