A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15588602



Internal ID4476404
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3560499..3572978hg38UCSC Ensembl
Innerchr17:3560999..3572478hg38UCSC Ensembl
Outerchr17:3559499..3573978hg38UCSC Ensembl
chr17:3463793..3476272hg19UCSC Ensembl
Innerchr17:3464293..3475772hg19UCSC Ensembl
Outerchr17:3462793..3477272hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3812480
hg1912480
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639745
Supporting Variants
SamplesHG03976
Known GenesTRPV1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15588602
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer