A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13835147



Internal ID1009388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:63339353..63340812hg38UCSC Ensembl
Innerchr10:63339357..63340809hg38UCSC Ensembl
Outerchr10:63339350..63340816hg38UCSC Ensembl
chr10:65099113..65100572hg19UCSC Ensembl
Innerchr10:65099117..65100569hg19UCSC Ensembl
Outerchr10:65099110..65100576hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg381460
hg191460
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623506
Supporting Variants
SamplesHG00631
Known GenesJMJD1C
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13835147
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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