A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13975497



Internal ID2050359
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:130491753..130506790hg38UCSC Ensembl
Innerchr10:130492253..130506290hg38UCSC Ensembl
Outerchr10:130490753..130507790hg38UCSC Ensembl
chr10:132290017..132305054hg19UCSC Ensembl
Innerchr10:132290517..132304554hg19UCSC Ensembl
Outerchr10:132289017..132306054hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg3815038
hg1915038
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624936
Supporting Variants
SamplesHG01872
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13975497
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