A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623806



Internal ID7010662
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:72943045..72949174hg38UCSC Ensembl
Innerchr10:72943075..72949145hg38UCSC Ensembl
Outerchr10:72943016..72949204hg38UCSC Ensembl
chr10:74702803..74708932hg19UCSC Ensembl
Innerchr10:74702833..74708903hg19UCSC Ensembl
Outerchr10:74702774..74708962hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg386130
hg196130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13861669
SamplesHG01107
Known GenesPLA2G12B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623806
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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