A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13848749



Internal ID3084714
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68202811..68206067hg38UCSC Ensembl
Innerchr10:68202837..68206041hg38UCSC Ensembl
Outerchr10:68202785..68206093hg38UCSC Ensembl
chr10:69962568..69965824hg19UCSC Ensembl
Innerchr10:69962594..69965798hg19UCSC Ensembl
Outerchr10:69962542..69965850hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg383257
hg193257
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623706
Supporting Variants
SamplesHG02703
Known GenesMYPN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13848749
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