A curated catalogue of human genomic structural variation




Variant Details

Variant: essv13935775



Internal ID3628933
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3624576
Supporting Variants
SamplesHG03228
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv13935775
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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