A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv701n100



Internal ID20152317
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:31321504..31388389hg38UCSC Ensembl
chr10:31610433..31677318hg19UCSC Ensembl
chr10:31650439..31717324hg18UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3866886
hg1966886
hg1866886
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1047471, nsv1042172, nsv1047554
Samples
Known GenesZEB1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv701n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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