A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1066677



Internal ID18809208
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43154674..43334601hg38UCSC Ensembl
Innerchr19:43658826..43838753hg19UCSC Ensembl
Innerchr19:48350666..48530593hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38179928
hg19179928
hg18179928
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3574187
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)nsv1066677
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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