A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4746



Internal ID15543231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:59076543..59092892hg38UCSC Ensembl
Outerchr4:59942261..59958610hg19UCSC Ensembl
Outerchr4:59624856..59641205hg18UCSC Ensembl
Outerchr4:59771027..59787376hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3816350
hg1916350
hg1816350
hg1716350
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4352
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)nssv4746
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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