A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2657294



Internal ID9576713
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:26964210..27423633hg38UCSC Ensembl
Outerchr17:26964176..27423668hg38UCSC Ensembl
Innerchr17:25291236..25750659hg19UCSC Ensembl
Outerchr17:25291202..25750694hg19UCSC Ensembl
Cytoband17q11.1
Allele length
AssemblyAllele length
hg38459493
hg19459493
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv540e199
Supporting Variantsessv5425454
SamplesHG00276
Known GenesMIR4522, TBC1D3P5, WSB1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
Comments
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2657294
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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