A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641204



Internal ID7027978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:72715700..72719385hg38UCSC Ensembl
Innerchr17:72716200..72718885hg38UCSC Ensembl
Outerchr17:72714700..72720385hg38UCSC Ensembl
chr17:70711839..70715524hg19UCSC Ensembl
Innerchr17:70712339..70715024hg19UCSC Ensembl
Outerchr17:70710839..70716524hg19UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg383686
hg193686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15735815
SamplesNA12348
Known GenesSLC39A11
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641204
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