A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3641062



Internal ID6681147
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:66308632..66312082hg38UCSC Ensembl
Innerchr17:66308652..66312062hg38UCSC Ensembl
Outerchr17:66308612..66312102hg38UCSC Ensembl
chr17:64304750..64308200hg19UCSC Ensembl
Innerchr17:64304770..64308180hg19UCSC Ensembl
Outerchr17:64304730..64308220hg19UCSC Ensembl
Cytoband17q24.2
Allele length
AssemblyAllele length
hg383451
hg193451
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv585e214
Supporting Variantsessv15725830
SamplesNA19923
Known GenesPRKCA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3641062
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