A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3646980



Internal ID7033722
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr21:36915597..36930895hg38UCSC Ensembl
chr21:38287897..38303195hg19UCSC Ensembl
Cytoband21q22.13
Allele length
AssemblyAllele length
hg3815299
hg1915299
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv814e214
Supporting Variantsessv16319823, essv16319821, essv16319822
SamplesHG00524, NA19383, NA18538
Known GenesHLCS
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3646980
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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