A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv135n100



Internal ID19010503
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25244339..25302128hg38UCSC Ensembl
chr1:25570830..25628619hg19UCSC Ensembl
chr1:25443417..25501206hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3857790
hg1957790
hg1857790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1014835, nsv1007623, nsv1004078, nsv998391
Samples
Known GenesC1orf63, RHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv135n100
Frequency
Sample Size29084
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


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