A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv31e55



Internal ID22760981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:57123412..57188447hg38UCSC Ensembl
chr10:58883172..58948207hg19UCSC Ensembl
chr10:58553178..58618213hg18UCSC Ensembl
chr10:58553178..58618213hg17UCSC Ensembl
Cytoband10q21.1
Allele length
AssemblyAllele length
hg3865036
hg1965036
hg1865036
hg1765036
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv34869, esv34583, esv34551, esv35059
SamplesNA18995, NA18572, NA18974, NA18564
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)dgv31e55
Frequency
Sample Size771
Observed Gain0
Observed Loss8
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer