A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4801



Internal ID15543133
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:183732500..183766388hg38UCSC Ensembl
Outerchr4:184653653..184687541hg19UCSC Ensembl
Outerchr4:184890647..184924535hg18UCSC Ensembl
Outerchr4:185028802..185062690hg17UCSC Ensembl
Cytoband4q35.1
Allele length
AssemblyAllele length
hg3833889
hg1933889
hg1833889
hg1733889
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4634
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)nssv4801
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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