A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv556e214



Internal ID22756450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:3560499..3573090hg38UCSC Ensembl
chr17:3463793..3476384hg19UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3812592
hg1912592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsesv3639747, esv3639745
SamplesHG03976, HG00266, NA19080
Known GenesTRPV1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)dgv556e214
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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