A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5943014



Internal ID8920417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124807082..124810995hg38UCSC Ensembl
chr10:126495651..126499564hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg383914
hg193914
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2660881
Supporting Variants
SamplesNA19080
Known GenesFAM175B
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5943014
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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