A curated catalogue of human genomic structural variation




Variant Details

Variant: essv5405892



Internal ID8383295
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:76284722..76285938hg38UCSC Ensembl
Outerchr17:76284565..76286091hg38UCSC Ensembl
Innerchr17:74280803..74282019hg19UCSC Ensembl
Outerchr17:74280646..74282172hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg381527
hg191527
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2673666
Supporting Variants
SamplesHG01171
Known GenesQRICH2
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)essv5405892
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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