A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623934



Internal ID6664101
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:79923186..80075168hg38UCSC Ensembl
chr10:81682942..81834924hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg38151983
hg19151983
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13870277, essv13870278, essv13870279
SamplesNA20339, NA19309, NA19312
Known GenesLOC100288974, SFTPD, TMEM254-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623934
Frequency
Sample Size2504
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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