A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv880n100



Internal ID22786967
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:65414695..65442030hg38UCSC Ensembl
chr10:67174453..67201788hg19UCSC Ensembl
chr10:66844459..66871794hg18UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg3827336
hg1927336
hg1827336
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1041309, nsv1047469
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)dgv880n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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