A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4413



Internal ID15202434
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:88083754..88129196hg38UCSC Ensembl
Outerchr4:89004906..89050348hg19UCSC Ensembl
Outerchr4:89223930..89269372hg18UCSC Ensembl
Outerchr4:89362085..89407527hg17UCSC Ensembl
Cytoband4q22.1
Allele length
AssemblyAllele length
hg3845443
hg1945443
hg1845443
hg1745443
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv7103
SamplesNA12156
Known GenesABCG2
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)nsv4413
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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