A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2677564



Internal ID9943669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr18:46397464..46398952hg38UCSC Ensembl
chr18:43977427..43978915hg19UCSC Ensembl
Cytoband18q21.1
Allele length
AssemblyAllele length
hg381489
hg191489
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6420117
SamplesNA18907
Known GenesRNF165
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2677564
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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