A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3639891



Internal ID7026669
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8766203..8768103hg38UCSC Ensembl
Innerchr17:8766203..8768103hg38UCSC Ensembl
Outerchr17:8765948..8768348hg38UCSC Ensembl
chr17:8669521..8671421hg19UCSC Ensembl
Innerchr17:8669521..8671421hg19UCSC Ensembl
Outerchr17:8669266..8671666hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15609340
SamplesHG00478
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3639891
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