A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640782



Internal ID7027556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:52399824..52400900hg38UCSC Ensembl
Innerchr17:52399874..52400808hg38UCSC Ensembl
Outerchr17:52399717..52401007hg38UCSC Ensembl
chr17:50477184..50478260hg19UCSC Ensembl
Innerchr17:50477234..50478168hg19UCSC Ensembl
Outerchr17:50477077..50478367hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg381077
hg191077
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15698755, essv15698754, essv15698763, essv15698753, essv15698760, essv15698759, essv15698762, essv15698756, essv15698758, essv15698757, essv15698761
SamplesHG03603, HG03943, HG03913, HG03817, HG03007, HG03636, HG04155, HG02696, HG03012, NA21095, HG03698
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640782
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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