A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061779



Internal ID18804310
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43159205..43338754hg38UCSC Ensembl
Innerchr19:43663357..43842906hg19UCSC Ensembl
Innerchr19:48355197..48534746hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38179550
hg19179550
hg18179550
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3574247, nssv3724625
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)nsv1061779
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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