A curated catalogue of human genomic structural variation




Variant Details

Variant: esv34541



Internal ID12643892
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:42828708..43301176hg38UCSC Ensembl
Innerchr19:43332860..43805328hg19UCSC Ensembl
Innerchr19:48024700..48497168hg18UCSC Ensembl
Innerchr19:48024700..48497168hg17UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg38472469
hg19472469
hg18472469
hg17472469
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv140e55
Supporting Variantsessv6979689, essv6979688, essv6979690, essv6990398
SamplesNA18605
Known GenesLOC284344, PSG1, PSG10P, PSG11, PSG2, PSG4, PSG5, PSG6, PSG7, PSG9
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv34541
Frequency
Sample Size771
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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