A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646725



Internal ID7033468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:25936719..25940010hg38UCSC Ensembl
Innerchr21:25936719..25940010hg38UCSC Ensembl
Outerchr21:25936613..25940107hg38UCSC Ensembl
chr21:27309033..27312324hg19UCSC Ensembl
Innerchr21:27309033..27312324hg19UCSC Ensembl
Outerchr21:27308927..27312421hg19UCSC Ensembl
Cytoband21q21.3
Allele length
AssemblyAllele length
hg383292
hg193292
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16297418
SamplesHG04098
Known GenesAPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646725
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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