A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3640221



Internal ID6680308
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:20913840..20955637hg38UCSC Ensembl
Innerchr17:20913840..20955637hg38UCSC Ensembl
Outerchr17:20913340..20956137hg38UCSC Ensembl
chr17:20817153..20858950hg19UCSC Ensembl
Innerchr17:20817153..20858950hg19UCSC Ensembl
Outerchr17:20816653..20859450hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3841798
hg1941798
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15650511
SamplesHG03072
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3640221
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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