A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064284



Internal ID18806815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35376040hg38UCSC Ensembl
Innerchr19:35849481..35866942hg19UCSC Ensembl
Innerchr19:40541321..40558782hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3817462
hg1917462
hg1817462
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3521n100
Supporting Variantsnssv3568145, nssv3568142, nssv3568144, nssv3568143, nssv3568140, nssv3568139, nssv3568141, nssv3724513
Samples
Known GenesFFAR3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1064284
Frequency
Sample Size29084
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


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