A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646977



Internal ID7033719
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36778899..36785490hg38UCSC Ensembl
Innerchr21:36778899..36785490hg38UCSC Ensembl
Outerchr21:36778794..36785738hg38UCSC Ensembl
chr21:38151200..38157791hg19UCSC Ensembl
Innerchr21:38151200..38157791hg19UCSC Ensembl
Outerchr21:38151095..38158039hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg386592
hg196592
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16319812, essv16319816, essv16319815, essv16319814, essv16319813
SamplesHG02589, NA19238, HG03461, HG03458, HG03445
Known GenesHLCS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646977
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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