A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv513013



Internal ID15505749
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:97899953..97901335hg38UCSC Ensembl
Outerchr10:99659710..99661092hg19UCSC Ensembl
Outerchr10:99649700..99651082hg18UCSC Ensembl
Cytoband10q24.2
Allele length
AssemblyAllele length
hg38718
hg19718
hg18718
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv625671
Samples1
Known GenesCRTAC1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nsv513013
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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