A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4515



Internal ID15549232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:132810439..132855772hg38UCSC Ensembl
Outerchr4:133731594..133776927hg19UCSC Ensembl
Outerchr4:133951044..133996377hg18UCSC Ensembl
Outerchr4:134089199..134134532hg17UCSC Ensembl
Cytoband4q28.3
Allele length
AssemblyAllele length
hg3845334
hg1945334
hg1845334
hg1745334
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7121
SamplesNA12156
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)nsv4515
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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