A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640318



Internal ID7027093
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:28987845..28998727hg38UCSC Ensembl
Innerchr17:28987845..28998727hg38UCSC Ensembl
Outerchr17:28987532..28999047hg38UCSC Ensembl
chr17:27314863..27325745hg19UCSC Ensembl
Innerchr17:27314863..27325745hg19UCSC Ensembl
Outerchr17:27314550..27326065hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg3810883
hg1910883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15656964
SamplesHG02379
Known GenesSEZ6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640318
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