A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4590



Internal ID15202629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:165855125..165888435hg38UCSC Ensembl
Outerchr4:166776277..166809587hg19UCSC Ensembl
Outerchr4:166995727..167029037hg18UCSC Ensembl
Outerchr4:167133882..167167192hg17UCSC Ensembl
Cytoband4q32.3
Allele length
AssemblyAllele length
hg386127
hg196127
hg186127
hg176127
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv8025
SamplesNA12156
Known GenesTLL1
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nsv4590
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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