A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626325



Internal ID15849858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:27852703..27855519hg38UCSC Ensembl
Outerchr1:28179214..28182030hg19UCSC Ensembl
Outerchr1:28051801..28054617hg18UCSC Ensembl
Cytoband1p35.3
Allele length
AssemblyAllele length
hg382817
hg192817
hg182817
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511686
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)nssv626325
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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