A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062590



Internal ID19151809
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43037255..43099219hg38UCSC Ensembl
Innerchr19:43541407..43603371hg19UCSC Ensembl
Innerchr19:48233247..48295211hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3861965
hg1961965
hg1861965
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3586n100
Supporting Variantsnssv3571753, nssv3723052, nssv3723051, nssv3571754
Samples
Known GenesPSG2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062590
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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