A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13919367



Internal ID3103927
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:105341005..105558140hg38UCSC Ensembl
Innerchr10:105341155..105557990hg38UCSC Ensembl
Outerchr10:105340855..105558290hg38UCSC Ensembl
chr10:107100763..107317898hg19UCSC Ensembl
Innerchr10:107100913..107317748hg19UCSC Ensembl
Outerchr10:107100613..107318048hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38217136
hg19217136
Variant TypeCNV gain
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624444
Supporting Variants
SamplesHG02725
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13919367
Frequency
Sample Size2504
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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