A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv8n97



Internal ID22815405
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:25256850..25346663hg38UCSC Ensembl
chr1:25583341..25673154hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg3889814
hg1989814
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1155377, nsv1155376
Samples
Known GenesRHD, TMEM50A
MethodSNP array
AnalysisDefault settings
Platform
Comments
ReferenceLou_et_al_2014
Pubmed ID25026903
Accession Number(s)dgv8n97
Frequency
Sample Size131
Observed Gain0
Observed Loss38
Observed Complex0
Frequencyn/a


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