A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv624728



Internal ID15848264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:52677994..52681821hg38UCSC Ensembl
Outerchr10:54437754..54441581hg19UCSC Ensembl
Outerchr10:54107760..54111587hg18UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg383828
hg193828
hg183828
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512164
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv624728
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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