A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055952



Internal ID18798483
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43148509..43352520hg38UCSC Ensembl
Innerchr19:43652661..43856672hg19UCSC Ensembl
Innerchr19:48344501..48548512hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38204012
hg19204012
hg18204012
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3591n100
Supporting Variantsnssv3571936
Samples
Known GenesLOC284344, PRG1, 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)nsv1055952
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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