A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2665419



Internal ID9584838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:48898838..48899112hg38UCSC Ensembl
chr10:50106883..50107157hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38275
hg19275
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv5425729, essv5747747, essv6458438, essv6093618, essv5865045
SamplesNA19712, NA18489, HG01384, NA19395, NA19818
Known GenesWDFY4
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2665419
Frequency
Sample Size1151
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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