A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626379



Internal ID15849912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:222376065..222377946hg38UCSC Ensembl
Outerchr1:222549407..222551288hg19UCSC Ensembl
Outerchr1:220616030..220617911hg18UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg381882
hg191882
hg181882
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511734
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626379
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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