A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625006



Internal ID15848542
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:100509764..100512205hg38UCSC Ensembl
Outerchr15:101049969..101052410hg19UCSC Ensembl
Outerchr15:98867492..98869933hg18UCSC Ensembl
Cytoband15q26.3
Allele length
AssemblyAllele length
hg382442
hg192442
hg182442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512415
Supporting Variants
Samples1
Known GenesCERS3
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625006
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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