A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv626516



Internal ID15850049
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:8680216..8728561hg38UCSC Ensembl
Outerchr3:8721902..8770247hg19UCSC Ensembl
Outerchr3:8696902..8745247hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3848346
hg1948346
hg1848346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv513034
Supporting Variants
Samples1
Known Genes
MethodSequencing
AnalysisAnalysis of HGMDFN090 by Illumina Genome Analyzer mate pairs
PlatformNot reported
Comments
ReferenceArlt_et_al_2011
Pubmed ID21212237
Accession Number(s)nssv626516
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