A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13785971



Internal ID3787787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:46319295..46322035hg38UCSC Ensembl
Innerchr10:46319322..46322008hg38UCSC Ensembl
Outerchr10:46319268..46322062hg38UCSC Ensembl
chr10:47690531..47693271hg19UCSC Ensembl
Innerchr10:47690558..47693244hg19UCSC Ensembl
Outerchr10:47690504..47693298hg19UCSC Ensembl
Cytoband10q11.22
Allele length
AssemblyAllele length
hg382741
hg192741
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623136
Supporting Variants
SamplesHG02667
Known GenesANTXRL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13785971
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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