A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062873



Internal ID18805404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358159..35370934hg38UCSC Ensembl
Innerchr19:35849061..35861836hg19UCSC Ensembl
Innerchr19:40540901..40553676hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812776
hg1912776
hg1812776
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3518n100
Supporting Variantsnssv3566606, nssv3566603, nssv3566611, nssv3566613, nssv3566615, nssv3566612, nssv3566617, nssv3566626, nssv3566607, nssv3566618, nssv3566623, nssv3566622, nssv3566610, nssv3566608, nssv3566609, nssv3566604, nssv3566624, nssv3566605, nssv3566627, nssv3566625, nssv3566614, nssv3566621, nssv3566602, nssv3566619, nssv3566620, nssv3566616
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)nsv1062873
Frequency
Sample Size29084
Observed Gain1
Observed Loss25
Observed Complex0
Frequencyn/a


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