A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568209



Internal ID18866490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:39866378..39921996hg38UCSC Ensembl
Innerchr19:40357018..40427903hg19UCSC Ensembl
Innerchr19:45048858..45119743hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3855619
hg1970886
hg1870886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1066339
Supporting Variants
Samples
Known GenesFCGBP
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568209
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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