A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624997



Internal ID15501847
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:77618181..77620049hg38UCSC Ensembl
Outerchr15:77910523..77912391hg19UCSC Ensembl
Outerchr15:75697578..75699446hg18UCSC Ensembl
Cytoband15q24.3
Allele length
AssemblyAllele length
hg381869
hg191869
hg181869
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512407
Supporting Variants
Samples1
Known GenesLINGO1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624997
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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