A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625496



Internal ID15849029
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr5:96515861..96516641hg38UCSC Ensembl
Outerchr5:95851565..95852345hg19UCSC Ensembl
Outerchr5:95877321..95878101hg18UCSC Ensembl
Cytoband5q15
Allele length
AssemblyAllele length
hg38935
hg19935
hg18935
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512855
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)nssv625496
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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