A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9391



Internal ID15540342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:34742526..34829507hg38UCSC Ensembl
Outerchr4:34744148..34831129hg19UCSC Ensembl
Outerchr4:34420543..34507524hg18UCSC Ensembl
Outerchr4:34566714..34653695hg17UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3886982
hg1986982
hg1886982
hg1786982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4295
Supporting Variants
SamplesNA18517
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)nssv9391
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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