A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3616169



Internal ID6656366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:9156160..9376889hg38UCSC Ensembl
chr8:9013670..9234399hg19UCSC Ensembl
Cytoband8p23.1
Allele length
AssemblyAllele length
hg38220730
hg19220730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1372e214
Supporting Variantsessv13095484
SamplesNA20761
Known GenesLOC157273
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3616169
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