A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055880



Internal ID19145099
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43001832..43225780hg38UCSC Ensembl
Innerchr19:43505984..43729932hg19UCSC Ensembl
Innerchr19:48197824..48421772hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38223949
hg19223949
hg18223949
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3577n100
Supporting Variantsnssv3571667
Samples
Known GenesLOC284344, PSG11, PSG2, PSG4, PSG5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055880
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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