A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6572606



Internal ID9511830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:224473802..224474599hg38UCSC Ensembl
chr1:224661504..224662301hg19UCSC Ensembl
Cytoband1q42.12
Allele length
AssemblyAllele length
hg38798
hg19798
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2670940
Supporting Variants
SamplesNA18990
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6572606
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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