A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6023783



Internal ID9251820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:150887787..150890334hg38UCSC Ensembl
chr1:150860263..150862810hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg382548
hg192548
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2658661
Supporting Variants
SamplesNA12144
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6023783
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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