A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6288221



Internal ID9265624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:169668500..169668660hg38UCSC Ensembl
chr1:169637738..169637898hg19UCSC Ensembl
Cytoband1q24.2
Allele length
AssemblyAllele length
hg38161
hg19161
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2667073
Supporting Variants
SamplesHG00251
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6288221
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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