A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv138e55



Internal ID22761088
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:22739747..23500295hg38UCSC Ensembl
chr19:22922549..23683097hg19UCSC Ensembl
chr19:22714389..23474937hg18UCSC Ensembl
chr19:22714389..23474937hg17UCSC Ensembl
Cytoband19p12
Allele length
AssemblyAllele length
hg38760549
hg19760549
hg18760549
hg17760549
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34907, esv34470
SamplesNA19145, NA19144
Known GenesLOC100132815, ZNF724P, ZNF728, ZNF730, ZNF91, ZNF99
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Affymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv138e55
Frequency
Sample Size771
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


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