A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3568796



Internal ID18867077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42751053..42864771hg38UCSC Ensembl
Innerchr19:43255205..43368923hg19UCSC Ensembl
Innerchr19:47947045..48060763hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38113719
hg19113719
hg18113719
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1059480
Supporting Variants
Samples
Known GenesLOC100289650, PSG10P, PSG8
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3568796
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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