A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625477



Internal ID15849010
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:155349236..155349484hg38UCSC Ensembl
Outerchr4:156270388..156270636hg19UCSC Ensembl
Outerchr4:156489838..156490086hg18UCSC Ensembl
Cytoband4q32.1
Allele length
AssemblyAllele length
hg381007
hg191007
hg181007
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512839
Supporting Variants
Samples1
Known GenesMAP9
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625477
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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