A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4458



Internal ID15549169
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:108108576..108153548hg38UCSC Ensembl
Outerchr4:109029732..109074704hg19UCSC Ensembl
Outerchr4:109249181..109294153hg18UCSC Ensembl
Outerchr4:109387336..109432308hg17UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg3844973
hg1944973
hg1844973
hg1744973
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7986
SamplesNA12156
Known GenesLEF1
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)nsv4458
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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