A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1058363



Internal ID19147582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42864771..43029369hg38UCSC Ensembl
Innerchr19:43368923..43533521hg19UCSC Ensembl
Innerchr19:48060763..48225361hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38164599
hg19164599
hg18164599
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3575n100
Supporting Variantsnssv3570134
Samples
Known GenesPSG1, PSG11, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1058363
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