A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13933343



Internal ID3935159
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:110030103..110031063hg38UCSC Ensembl
Innerchr10:110030106..110031060hg38UCSC Ensembl
Outerchr10:110030100..110031066hg38UCSC Ensembl
chr10:111789861..111790821hg19UCSC Ensembl
Innerchr10:111789864..111790818hg19UCSC Ensembl
Outerchr10:111789858..111790824hg19UCSC Ensembl
Cytoband10q25.1
Allele length
AssemblyAllele length
hg38961
hg19961
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624532
Supporting Variants
SamplesHG03976
Known GenesADD3
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13933343
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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