A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6116092



Internal ID9093495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:176829919..176830128hg38UCSC Ensembl
Outerchr5:176829882..176830178hg38UCSC Ensembl
Innerchr5:176256920..176257129hg19UCSC Ensembl
Outerchr5:176256883..176257179hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2666951
Supporting Variants
SamplesNA19920
Known GenesUNC5A
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6116092
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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