A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640224



Internal ID6680311
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20957522..20982745hg38UCSC Ensembl
Innerchr17:20957522..20982745hg38UCSC Ensembl
Outerchr17:20957022..20983245hg38UCSC Ensembl
chr17:20860835..20886058hg19UCSC Ensembl
Innerchr17:20860835..20886058hg19UCSC Ensembl
Outerchr17:20860335..20886558hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3825224
hg1925224
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15650659
SamplesHG03476
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640224
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