A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv139n100



Internal ID20151755
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25269444..25320443hg38UCSC Ensembl
chr1:25595935..25646934hg19UCSC Ensembl
chr1:25468522..25519521hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3851000
hg1951000
hg1851000
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1013309, nsv1012128
Samples
Known GenesRHD
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv139n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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