A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13689285



Internal ID5406770
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7133146..7136178hg38UCSC Ensembl
Innerchr10:7133156..7136169hg38UCSC Ensembl
Outerchr10:7133137..7136188hg38UCSC Ensembl
chr10:7175108..7178140hg19UCSC Ensembl
Innerchr10:7175118..7178131hg19UCSC Ensembl
Outerchr10:7175099..7178150hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg383033
hg193033
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622267
Supporting Variants
SamplesNA18946
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13689285
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