A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639748



Internal ID7026526
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3562752..3573090hg38UCSC Ensembl
chr17:3466046..3476384hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3810339
hg1910339
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15588610, essv15588608, essv15588609
SamplesHG02820, HG02768, HG01631
Known GenesTRPV1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639748
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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