A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5528211



Internal ID9722126
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:4968077..4996214hg38UCSC Ensembl
Outerchr1:4968043..4996249hg38UCSC Ensembl
Innerchr1:5028137..5056274hg19UCSC Ensembl
Outerchr1:5028103..5056309hg19UCSC Ensembl
Cytoband1p36.32
Allele length
AssemblyAllele length
hg3828207
hg1928207
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2674284
Supporting Variants
SamplesNA19473
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5528211
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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