A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646989



Internal ID7033731
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:37335081..37339523hg38UCSC Ensembl
Innerchr21:37335108..37339496hg38UCSC Ensembl
Outerchr21:37335054..37339550hg38UCSC Ensembl
chr21:38707383..38711825hg19UCSC Ensembl
Innerchr21:38707410..38711798hg19UCSC Ensembl
Outerchr21:38707356..38711852hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg384443
hg194443
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16319964, essv16319962, essv16319966, essv16319963, essv16319965
SamplesNA19446, HG03572, NA19449, NA19435, NA19328
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646989
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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