A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626838



Internal ID15503685
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr22:25819941..25820054hg38UCSC Ensembl
Outerchr22:26215908..26216021hg19UCSC Ensembl
Outerchr22:24545908..24546021hg18UCSC Ensembl
Cytoband22q12.1
Allele length
AssemblyAllele length
hg381157
hg191157
hg181157
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513586
Supporting Variants
Samples1
Known GenesMIR1302-1, MYO18B
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626838
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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