A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15724801



Internal ID3847293
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:65125356..65126547hg38UCSC Ensembl
Innerchr17:65125392..65126511hg38UCSC Ensembl
Outerchr17:65125320..65126583hg38UCSC Ensembl
chr17:63121474..63122665hg19UCSC Ensembl
Innerchr17:63121510..63122629hg19UCSC Ensembl
Outerchr17:63121438..63122701hg19UCSC Ensembl
Cytoband17q24.1
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641037
Supporting Variants
SamplesHG03479
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15724801
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