A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv705n100



Internal ID20152321
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34871114..35045560hg38UCSC Ensembl
chr10:35160042..35334488hg19UCSC Ensembl
chr10:35200048..35374494hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38174447
hg19174447
hg18174447
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1053144, nsv1051496, nsv1037134, nsv1040417
Samples
Known GenesCUL2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv705n100
Frequency
Sample Size29084
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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