A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626470



Internal ID15503317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr2:152603064..152605020hg38UCSC Ensembl
Outerchr2:153459578..153461534hg19UCSC Ensembl
Outerchr2:153167824..153169780hg18UCSC Ensembl
Cytoband2q23.3
Allele length
AssemblyAllele length
hg381957
hg191957
hg181957
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511817
Supporting Variants
Samples1
Known GenesFMNL2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626470
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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