A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5928491



Internal ID9651368
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:244729423..244736914hg38UCSC Ensembl
chr1:244892725..244900216hg19UCSC Ensembl
Cytoband1q44
Allele length
AssemblyAllele length
hg387492
hg197492
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2676327
Supporting Variants
SamplesNA19382
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5928491
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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