A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv657n100



Internal ID22786744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:1892181..1950452hg38UCSC Ensembl
chr10:1934375..1992646hg19UCSC Ensembl
chr10:1924375..1982646hg18UCSC Ensembl
Cytoband10p15.3
Allele length
AssemblyAllele length
hg3858272
hg1958272
hg1858272
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1037341, nsv1038809, nsv1051720
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv657n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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