A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640359



Internal ID7027134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:31065095..31070767hg38UCSC Ensembl
Innerchr17:31065125..31070737hg38UCSC Ensembl
Outerchr17:31065065..31070797hg38UCSC Ensembl
chr17:29392113..29397785hg19UCSC Ensembl
Innerchr17:29392143..29397755hg19UCSC Ensembl
Outerchr17:29392083..29397815hg19UCSC Ensembl
Cytoband17q11.2
Allele length
AssemblyAllele length
hg385673
hg195673
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15657897
SamplesNA20881
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640359
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