A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1064016



Internal ID18806547
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358579..35370793hg38UCSC Ensembl
Innerchr19:35849481..35861695hg19UCSC Ensembl
Innerchr19:40541321..40553535hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812215
hg1912215
hg1812215
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3519n100
Supporting Variantsnssv3566665, nssv3566662, nssv3566663, nssv3566666, nssv3566661, nssv3724361, nssv3724363, nssv3724362, nssv3724364, nssv3566664
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)nsv1064016
Frequency
Sample Size29084
Observed Gain0
Observed Loss10
Observed Complex0
Frequencyn/a


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