A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4725



Internal ID15196581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:8620980..8635538hg38UCSC Ensembl
Outerchr4:8622706..8637264hg19UCSC Ensembl
Outerchr4:8673606..8688164hg18UCSC Ensembl
Outerchr4:8740777..8755335hg17UCSC Ensembl
Cytoband4p16.1
Allele length
AssemblyAllele length
hg3814559
hg1914559
hg1814559
hg1714559
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4226
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)nssv4725
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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