A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv134n100



Internal ID20151750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25232069..25320483hg38UCSC Ensembl
chr1:25558560..25646974hg19UCSC Ensembl
chr1:25431147..25519561hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3888415
hg1988415
hg1888415
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1005659, nsv998556, nsv1003163, nsv1006870, nsv1010825, nsv1006754, nsv999496
Samples
Known GenesC1orf63, RHD, SYF2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv134n100
Frequency
Sample Size29084
Observed Gain37
Observed Loss0
Observed Complex0
Frequencyn/a


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