A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13837748



Internal ID1321957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64882381..64889608hg38UCSC Ensembl
Innerchr10:64882381..64889608hg38UCSC Ensembl
Outerchr10:64882128..64889667hg38UCSC Ensembl
chr10:66642138..66649365hg19UCSC Ensembl
Innerchr10:66642138..66649365hg19UCSC Ensembl
Outerchr10:66641885..66649424hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg387228
hg197228
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3623545
Supporting Variants
SamplesHG01168
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13837748
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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