A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13690316



Internal ID4384134
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:8304777..8312695hg38UCSC Ensembl
Innerchr10:8304802..8312670hg38UCSC Ensembl
Outerchr10:8304752..8312720hg38UCSC Ensembl
chr10:8346740..8354658hg19UCSC Ensembl
Innerchr10:8346765..8354633hg19UCSC Ensembl
Outerchr10:8346715..8354683hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg387919
hg197919
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3622285
Supporting Variants
SamplesHG03908
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13690316
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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