A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13953785



Internal ID4722854
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:121673690..121701978hg38UCSC Ensembl
Innerchr10:121674190..121701478hg38UCSC Ensembl
Outerchr10:121672690..121702978hg38UCSC Ensembl
chr10:123433204..123461492hg19UCSC Ensembl
Innerchr10:123433704..123460992hg19UCSC Ensembl
Outerchr10:123432204..123462492hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg3828289
hg1928289
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624756
Supporting Variants
SamplesNA06984
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13953785
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