A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626078



Internal ID15849611
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:131111671..131114439hg38UCSC Ensembl
Outerchr10:131110205..131116646hg38UCSC Ensembl
Innerchr10:132909934..132912702hg19UCSC Ensembl
Outerchr10:132908468..132914909hg19UCSC Ensembl
Innerchr10:132799924..132802692hg18UCSC Ensembl
Outerchr10:132798458..132804899hg18UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg386442
hg196442
hg186442
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511463
Supporting Variants
Samples1
Known GenesTCERG1L
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626078
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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