A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4566



Internal ID15549288
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155974781..156019118hg38UCSC Ensembl
Outerchr4:156895933..156940270hg19UCSC Ensembl
Outerchr4:157115383..157159720hg18UCSC Ensembl
Outerchr4:157253538..157297875hg17UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg3844338
hg1944338
hg1844338
hg1744338
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2491
SamplesNA18555
Known Genes
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)nsv4566
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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