A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3647308



Internal ID6687363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr22:21008293..21023987hg38UCSC Ensembl
Innerchr22:21008793..21023487hg38UCSC Ensembl
Outerchr22:21007293..21024987hg38UCSC Ensembl
chr22:21362582..21378276hg19UCSC Ensembl
Innerchr22:21363082..21377776hg19UCSC Ensembl
Outerchr22:21361582..21379276hg19UCSC Ensembl
Cytoband22q11.21
Allele length
AssemblyAllele length
hg3815695
hg1915695
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv16370919, essv16370918
SamplesHG00282, HG02013
Known GenesP2RX6, THAP7-AS1, TUBA3FP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3647308
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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