A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13848640



Internal ID2407716
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:68010163..68010841hg38UCSC Ensembl
Innerchr10:68010181..68010824hg38UCSC Ensembl
Outerchr10:68010146..68010859hg38UCSC Ensembl
chr10:69769920..69770598hg19UCSC Ensembl
Innerchr10:69769938..69770581hg19UCSC Ensembl
Outerchr10:69769903..69770616hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg38679
hg19679
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623700
Supporting Variants
SamplesHG02134
Known GenesHERC4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13848640
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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