A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2671936



Internal ID9938041
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75185992..75203995hg38UCSC Ensembl
chr17:73182087..73200090hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg3818004
hg1918004
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6501135
SamplesNA20798
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2671936
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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