A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv625620



Internal ID15502467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:133213115..133214317hg38UCSC Ensembl
Outerchr8:134225358..134226560hg19UCSC Ensembl
Outerchr8:134294540..134295742hg18UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg38889
hg19889
hg18889
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv512967
Supporting Variants
Samples1
Known GenesWISP1
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv625620
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer