A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623028



Internal ID7009885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:42772589..42828520hg38UCSC Ensembl
Innerchr10:42772589..42828520hg38UCSC Ensembl
Outerchr10:42772089..42829020hg38UCSC Ensembl
chr10:43268037..43323968hg19UCSC Ensembl
Innerchr10:43268037..43323968hg19UCSC Ensembl
Outerchr10:43267537..43324468hg19UCSC Ensembl
Cytoband10q11.21
Allele length
AssemblyAllele length
hg3855932
hg1955932
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13764209
SamplesNA18620
Known GenesBMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623028
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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