A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6375325



Internal ID9352728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:77933125..77933913hg38UCSC Ensembl
Outerchr17:77933086..77933970hg38UCSC Ensembl
Innerchr17:75929207..75929995hg19UCSC Ensembl
Outerchr17:75929168..75930052hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38885
hg19885
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsesv2668003
Supporting Variants
SamplesNA18549
Known Genes
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv6375325
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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