A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv7116



Internal ID15190062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:114575940..114597470hg38UCSC Ensembl
Outerchr4:115497096..115518626hg19UCSC Ensembl
Outerchr4:115716545..115738075hg18UCSC Ensembl
Outerchr4:115854700..115876230hg17UCSC Ensembl
Cytoband4q26
Allele length
AssemblyAllele length
hg3821531
hg1921531
hg1821531
hg1721531
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv4478
Supporting Variants
SamplesNA12156
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)nssv7116
Frequency
Sample Size9
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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