A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626335



Internal ID15503182
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:63239617..63242492hg38UCSC Ensembl
Outerchr1:63705288..63708163hg19UCSC Ensembl
Outerchr1:63477876..63480751hg18UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg382876
hg192876
hg182876
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511695
Supporting Variants
Samples1
Known GenesLINC00466
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626335
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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