A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6221301



Internal ID8952341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:177011179..177012545hg38UCSC Ensembl
Outerchr5:177011022..177012698hg38UCSC Ensembl
Innerchr5:176438180..176439546hg19UCSC Ensembl
Outerchr5:176438023..176439699hg19UCSC Ensembl
Cytoband5q35.2
Allele length
AssemblyAllele length
hg381677
hg191677
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2661861
Supporting Variants
SamplesHG00501
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6221301
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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