A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv21e55



Internal ID20126500
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:44699737..44861146hg38UCSC Ensembl
chr10:45195185..45356594hg19UCSC Ensembl
chr10:44515191..44676600hg18UCSC Ensembl
chr10:44515191..44676600hg17UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg38161410
hg19161410
hg18161410
hg17161410
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2750893, esv2750894, esv2750896, esv2750895
SamplesBEC_428, BEC_675, BEC_830, BEC_554
Known GenesTMEM72-AS1
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)dgv21e55
Frequency
Sample Size771
Observed Gain18
Observed Loss0
Observed Complex0
Frequencyn/a


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