A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624762



Internal ID15848298
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:133291151..133292495hg38UCSC Ensembl
Outerchr10:135104655..135105999hg19UCSC Ensembl
Outerchr10:134954645..134955989hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381345
hg191345
hg181345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512195
Supporting Variants
Samples1
Known GenesTUBGCP2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624762
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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