A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622479



Internal ID7009338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17035822..17037203hg38UCSC Ensembl
Innerchr10:17035852..17037173hg38UCSC Ensembl
Outerchr10:17035792..17037233hg38UCSC Ensembl
chr10:17077821..17079202hg19UCSC Ensembl
Innerchr10:17077851..17079172hg19UCSC Ensembl
Outerchr10:17077791..17079232hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg381382
hg191382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13706545
SamplesNA19024
Known GenesCUBN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622479
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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