A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1060137



Internal ID18802668
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43154674..43335547hg38UCSC Ensembl
Innerchr19:43658826..43839699hg19UCSC Ensembl
Innerchr19:48350666..48531539hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38180874
hg19180874
hg18180874
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3574188
Samples
Known GenesLOC284344, PSG4, PSG5, PSG9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1060137
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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