A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1059734



Internal ID18802265
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:54073048..54097891hg38UCSC Ensembl
Innerchr19:54576302..54601174hg19UCSC Ensembl
Innerchr19:59268114..59292986hg18UCSC Ensembl
Cytoband19q13.42
Allele length
AssemblyAllele length
hg3824844
hg1924873
hg1824873
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3653n100
Supporting Variantsnssv3573308, nssv3573307
Samples
Known GenesOSCAR, TARM1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1059734
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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