A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626676



Internal ID15850209
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:188015548..188016985hg38UCSC Ensembl
Outerchr3:188009727..188017899hg38UCSC Ensembl
Innerchr3:187733336..187734773hg19UCSC Ensembl
Outerchr3:187727515..187735687hg19UCSC Ensembl
Innerchr3:189216030..189217467hg18UCSC Ensembl
Outerchr3:189210209..189218381hg18UCSC Ensembl
Cytoband3q27.3
Allele length
AssemblyAllele length
hg388173
hg198173
hg188173
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv511211
Supporting Variants
Samples1
Known Genes
MethodSNP array
AnalysisAnalysis of HGMDFN090 by Illumina HumanOmni1 Quad SNP array
PlatformGPL8882
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626676
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