A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv34e55



Internal ID22760984
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105845347..105924200hg38UCSC Ensembl
chr10:107605105..107683958hg19UCSC Ensembl
chr10:107595095..107673948hg18UCSC Ensembl
chr10:107595095..107673948hg17UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg3878854
hg1978854
hg1878854
hg1778854
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2750849, esv34654
SamplesBEC_547, NA06991
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv34e55
Frequency
Sample Size771
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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