A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv136n100



Internal ID20151752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25247968..25336807hg38UCSC Ensembl
chr1:25574459..25663298hg19UCSC Ensembl
chr1:25447046..25535885hg18UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3888840
hg1988840
hg1888840
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1003885, nsv1011605, nsv1014241, nsv1011672, nsv1007231
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)dgv136n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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