A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625532



Internal ID15849065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:89872110..89872393hg38UCSC Ensembl
Outerchr6:90581829..90582112hg19UCSC Ensembl
Outerchr6:90638550..90638833hg18UCSC Ensembl
Cytoband6q15
Allele length
AssemblyAllele length
hg382135
hg192135
hg182135
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512888
Supporting Variants
Samples1
Known GenesCASP8AP2
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625532
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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