A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4556



Internal ID15202591
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:153161079..153197065hg38UCSC Ensembl
Outerchr4:154082231..154118217hg19UCSC Ensembl
Outerchr4:154301681..154337667hg18UCSC Ensembl
Outerchr4:154439836..154475822hg17UCSC Ensembl
Cytoband4q31.3
Allele length
AssemblyAllele length
hg386252
hg196252
hg186252
hg176252
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3139, nssv4790
SamplesNA19129, NA18555
Known GenesTRIM2
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)nsv4556
Frequency
Sample Size9
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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