A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646952



Internal ID7033694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:35832670..35840132hg38UCSC Ensembl
Innerchr21:35832677..35840126hg38UCSC Ensembl
Outerchr21:35832664..35840139hg38UCSC Ensembl
chr21:37204968..37212430hg19UCSC Ensembl
Innerchr21:37204975..37212424hg19UCSC Ensembl
Outerchr21:37204962..37212437hg19UCSC Ensembl
Cytoband21q22.12
Allele length
AssemblyAllele length
hg387463
hg197463
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16317403
SamplesNA19428
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646952
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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