A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6025022



Internal ID9002425
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:154233510..154233936hg38UCSC Ensembl
chr1:154205986..154206412hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg38427
hg19427
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2672763
Supporting Variants
SamplesNA19213
Known GenesUBAP2L
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6025022
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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