A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv704n100



Internal ID19011072
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34771494..34859811hg38UCSC Ensembl
chr10:35060422..35148739hg19UCSC Ensembl
chr10:35100428..35188745hg18UCSC Ensembl
Cytoband10p11.21
Allele length
AssemblyAllele length
hg3888318
hg1988318
hg1888318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1049119, nsv1042403
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)dgv704n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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