A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624576



Internal ID7011429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:112236358..112241488hg38UCSC Ensembl
Innerchr10:112236369..112241478hg38UCSC Ensembl
Outerchr10:112236348..112241499hg38UCSC Ensembl
chr10:113996116..114001246hg19UCSC Ensembl
Innerchr10:113996127..114001236hg19UCSC Ensembl
Outerchr10:113996106..114001257hg19UCSC Ensembl
Cytoband10q25.2
Allele length
AssemblyAllele length
hg385131
hg195131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13935775, essv13935774, essv13935773, essv13935776, essv13935778, essv13935777
SamplesHG03228, HG00151, NA20894, HG00117, HG04093, HG03867
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624576
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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