A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4784



Internal ID15543162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:145993864..146012221hg38UCSC Ensembl
Outerchr4:146915016..146933373hg19UCSC Ensembl
Outerchr4:147134466..147152823hg18UCSC Ensembl
Outerchr4:147272621..147290978hg17UCSC Ensembl
Cytoband4q31.22
Allele length
AssemblyAllele length
hg3818358
hg1918358
hg1818358
hg1718358
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4535
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)nssv4784
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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