A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624992



Internal ID15848528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr15:70728813..70735254hg38UCSC Ensembl
Outerchr15:71021152..71027593hg19UCSC Ensembl
Outerchr15:68808206..68814647hg18UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg386442
hg196442
hg186442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512402
Supporting Variants
Samples1
Known GenesUACA
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624992
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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