A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641269



Internal ID7028043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:75885307..75894398hg38UCSC Ensembl
Innerchr17:75885307..75894398hg38UCSC Ensembl
Outerchr17:75884807..75894898hg38UCSC Ensembl
chr17:73881388..73890479hg19UCSC Ensembl
Innerchr17:73881388..73890479hg19UCSC Ensembl
Outerchr17:73880888..73890979hg19UCSC Ensembl
Cytoband17q25.1
Allele length
AssemblyAllele length
hg389092
hg199092
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15740832, essv15740833
SamplesHG01259, HG01432
Known GenesTRIM65
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641269
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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