A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2662311



Internal ID9928416
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3561202..3568311hg38UCSC Ensembl
chr17:3464496..3471605hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg387110
hg197110
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6003648
SamplesHG00464
Known GenesTRPV1
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2662311
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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