A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv138n100



Internal ID19010506
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25256340..25320483hg38UCSC Ensembl
chr1:25582831..25646974hg19UCSC Ensembl
chr1:25455418..25519561hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3864144
hg1964144
hg1864144
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1010467, nsv1011563, nsv1008344, nsv1006617, nsv1011287, nsv1009320, nsv1007934
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)dgv138n100
Frequency
Sample Size29084
Observed Gain406
Observed Loss690
Observed Complex0
Frequencyn/a


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