A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623773



Internal ID7010629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:71370570..71378319hg38UCSC Ensembl
Innerchr10:71370570..71378319hg38UCSC Ensembl
Outerchr10:71370070..71378819hg38UCSC Ensembl
chr10:73130327..73138076hg19UCSC Ensembl
Innerchr10:73130327..73138076hg19UCSC Ensembl
Outerchr10:73129827..73138576hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387750
hg197750
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13859552
SamplesNA20357
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623773
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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