A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625685



Internal ID15502532
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:129518445..129518561hg38UCSC Ensembl
Outerchr10:131316709..131316825hg19UCSC Ensembl
Outerchr10:131206699..131206815hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381095
hg191095
hg181095
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513300
Supporting Variants
Samples1
Known GenesMGMT
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625685
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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