A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13932799



Internal ID2924835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:107647903..107656203hg38UCSC Ensembl
Innerchr10:107647911..107656195hg38UCSC Ensembl
Outerchr10:107647895..107656211hg38UCSC Ensembl
chr10:109407661..109415961hg19UCSC Ensembl
Innerchr10:109407669..109415953hg19UCSC Ensembl
Outerchr10:109407653..109415969hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg388301
hg198301
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624489
Supporting Variants
SamplesHG02586
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13932799
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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