A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13742912



Internal ID3744728
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29453284..29454006hg38UCSC Ensembl
Innerchr10:29453296..29453995hg38UCSC Ensembl
Outerchr10:29453273..29454018hg38UCSC Ensembl
chr10:29742213..29742935hg19UCSC Ensembl
Innerchr10:29742225..29742924hg19UCSC Ensembl
Outerchr10:29742202..29742947hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38723
hg19723
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622773
Supporting Variants
SamplesNA12750
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13742912
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