A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647077



Internal ID7033819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:42024500..42027168hg38UCSC Ensembl
Innerchr21:42024550..42027118hg38UCSC Ensembl
Outerchr21:42024399..42027269hg38UCSC Ensembl
chr21:43444609..43447277hg19UCSC Ensembl
Innerchr21:43444659..43447227hg19UCSC Ensembl
Outerchr21:43444508..43447378hg19UCSC Ensembl
Cytoband21q22.3
Allele length
AssemblyAllele length
hg382669
hg192669
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16324734
SamplesHG01986
Known GenesZNF295-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647077
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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