A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13945775



Internal ID4438450
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:115974589..115980039hg38UCSC Ensembl
Innerchr10:115974625..115980003hg38UCSC Ensembl
Outerchr10:115974553..115980075hg38UCSC Ensembl
chr10:117734100..117739550hg19UCSC Ensembl
Innerchr10:117734136..117739514hg19UCSC Ensembl
Outerchr10:117734064..117739586hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg385451
hg195451
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624648
Supporting Variants
SamplesHG03947
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13945775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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