A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622504



Internal ID6662674
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:18325115..18325934hg38UCSC Ensembl
Innerchr10:18325127..18325922hg38UCSC Ensembl
Outerchr10:18325103..18325946hg38UCSC Ensembl
chr10:18614044..18614863hg19UCSC Ensembl
Innerchr10:18614056..18614851hg19UCSC Ensembl
Outerchr10:18614032..18614875hg19UCSC Ensembl
Cytoband10p12.32
Allele length
AssemblyAllele length
hg38820
hg19820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13710152, essv13710153
SamplesNA19834, NA19914
Known GenesCACNB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622504
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer