A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624790



Internal ID6664951
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:122963967..122970460hg38UCSC Ensembl
Innerchr10:122963987..122970440hg38UCSC Ensembl
Outerchr10:122963947..122970480hg38UCSC Ensembl
chr10:124723483..124729976hg19UCSC Ensembl
Innerchr10:124723503..124729956hg19UCSC Ensembl
Outerchr10:124723463..124729996hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg386494
hg196494
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13958181
SamplesNA19201
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624790
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