A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3624826



Internal ID7011676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:125191905..125193426hg38UCSC Ensembl
Innerchr10:125191905..125193426hg38UCSC Ensembl
Outerchr10:125191623..125193660hg38UCSC Ensembl
chr10:126880474..126881995hg19UCSC Ensembl
Innerchr10:126880474..126881995hg19UCSC Ensembl
Outerchr10:126880192..126882229hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg381522
hg191522
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13963549, essv13963548, essv13963546, essv13963545, essv13963547, essv13963550
SamplesNA19028, NA19446, NA19385, NA19035, NA19435, NA19430
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3624826
Frequency
Sample Size2504
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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