A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2675441



Internal ID9941546
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:796739..801576hg38UCSC Ensembl
Outerchr17:796702..801626hg38UCSC Ensembl
Innerchr17:699979..704816hg19UCSC Ensembl
Outerchr17:699942..704866hg19UCSC Ensembl
Cytoband17p13.3
Allele length
AssemblyAllele length
hg384925
hg194925
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6052085
SamplesNA18617
Known GenesNXN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2675441
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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