A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624813



Internal ID7011663
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:124546406..124546999hg38UCSC Ensembl
Innerchr10:124546456..124546949hg38UCSC Ensembl
Outerchr10:124546344..124547061hg38UCSC Ensembl
chr10:126234975..126235568hg19UCSC Ensembl
Innerchr10:126235025..126235518hg19UCSC Ensembl
Outerchr10:126234913..126235630hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38594
hg19594
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963287
SamplesNA19004
Known GenesLHPP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624813
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