A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4669



Internal ID15543168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8502000..8544735hg38UCSC Ensembl
Outerchr4:8503727..8546462hg19UCSC Ensembl
Outerchr4:8554627..8597362hg18UCSC Ensembl
Outerchr4:8621798..8664533hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3842736
hg1942736
hg1842736
hg1742736
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4224
Supporting Variants
SamplesNA19129
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)nssv4669
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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