A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15609338



Internal ID1509983
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:8681061..8682259hg38UCSC Ensembl
Innerchr17:8681061..8682259hg38UCSC Ensembl
Outerchr17:8680859..8682447hg38UCSC Ensembl
chr17:8584379..8585577hg19UCSC Ensembl
Innerchr17:8584379..8585577hg19UCSC Ensembl
Outerchr17:8584177..8585765hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg381199
hg191199
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3639889
Supporting Variants
SamplesHG01389
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15609338
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