A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv499050



Internal ID15815146
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:79966892..79972954hg38UCSC Ensembl
chr4:80888046..80894108hg19UCSC Ensembl
chr4:81107070..81113132hg18UCSC Ensembl
Cytoband4q21.21
Allele length
AssemblyAllele length
hg386063
hg196063
hg186063
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv585911
Samples
Known GenesANTXR2
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)nsv499050
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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