A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4438



Internal ID15549147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:99029503..99063090hg38UCSC Ensembl
Outerchr4:99950654..99984241hg19UCSC Ensembl
Outerchr4:100169677..100203264hg18UCSC Ensembl
Outerchr4:100307832..100341419hg17UCSC Ensembl
Cytoband4q23
Allele length
AssemblyAllele length
hg385697
hg195697
hg185697
hg175697
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv4771
SamplesNA19129
Known GenesMETAP1
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)nsv4438
Frequency
Sample Size9
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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