A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv702n100



Internal ID19011070
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34697315..34925688hg38UCSC Ensembl
chr10:34986243..35214616hg19UCSC Ensembl
chr10:35026249..35254622hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg38228374
hg19228374
hg18228374
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1046127, nsv1038748
Samples
Known GenesPARD3, PARD3-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv702n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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