A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv3574n100



Internal ID22789661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:42811447..43065876hg38UCSC Ensembl
chr19:43315599..43570028hg19UCSC Ensembl
chr19:48007439..48261868hg18UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38254430
hg19254430
hg18254430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1059288, nsv1065857, nsv1064203, nsv1057231, nsv1058401, nsv1062084
Samples
Known GenesLOC100289650, PSG1, PSG10P, PSG11, PSG2, PSG6, PSG7
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv3574n100
Frequency
Sample Size11257
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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