A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059305



Internal ID18801836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:19020501..19099190hg38UCSC Ensembl
Innerchr19:19131310..19209999hg19UCSC Ensembl
Innerchr19:18992310..19070999hg18UCSC Ensembl
Cytoband19p13.11
Allele length
AssemblyAllele length
hg3878690
hg1978690
hg1878690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3569785
Samples
Known GenesARMC6, SLC25A42, SUGP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059305
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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