A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv267e55



Internal ID22761217
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chrX:7425903..7540555hg38UCSC Ensembl
chrX:7343944..7458596hg19UCSC Ensembl
chrX:7353944..7468596hg18UCSC Ensembl
chrX:7203680..7318332hg17UCSC Ensembl
CytobandXp22.31
Allele length
AssemblyAllele length
hg38114653
hg19114653
hg18114653
hg17114653
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv2752333, esv34462
SamplesBEC_341, NA12248
Known Genes
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)dgv267e55
Frequency
Sample Size771
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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