A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056390



Internal ID19145609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42864771..43038667hg38UCSC Ensembl
Innerchr19:43368923..43542819hg19UCSC Ensembl
Innerchr19:48060763..48234659hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38173897
hg19173897
hg18173897
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3575n100
Supporting Variantsnssv3570135, nssv3723029, nssv3570136, nssv3570137
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)nsv1056390
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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