A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15753385



Internal ID5755201
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:79690513..79705379hg38UCSC Ensembl
chr17:77664437..77679188hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3814867
hg1914752
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3641352
Supporting Variants
SamplesHG02733
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15753385
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