A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1065890



Internal ID18808421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:35358395..35370934hg38UCSC Ensembl
Innerchr19:35849297..35861836hg19UCSC Ensembl
Innerchr19:40541137..40553676hg18UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg3812540
hg1912540
hg1812540
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3519n100
Supporting Variantsnssv3724359, nssv3566646, nssv3566654, nssv3724360, nssv3566647, nssv3566650, nssv3724358, nssv3566652, nssv3566649, nssv3566645, nssv3566651, nssv3566648, nssv3566655, nssv3566644, nssv3566643, nssv3566653, nssv3566642
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)nsv1065890
Frequency
Sample Size29084
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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