A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623766



Internal ID7010622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:70612289..70627158hg38UCSC Ensembl
Innerchr10:70612789..70626658hg38UCSC Ensembl
Outerchr10:70611289..70628158hg38UCSC Ensembl
chr10:72372045..72386914hg19UCSC Ensembl
Innerchr10:72372545..72386414hg19UCSC Ensembl
Outerchr10:72371045..72387914hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg3814870
hg1914870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13858619
SamplesHG02887
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623766
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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