A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623521



Internal ID7010377
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:64222007..64227813hg38UCSC Ensembl
Innerchr10:64222008..64227812hg38UCSC Ensembl
Outerchr10:64222006..64227814hg38UCSC Ensembl
chr10:65981767..65987573hg19UCSC Ensembl
Innerchr10:65981768..65987572hg19UCSC Ensembl
Outerchr10:65981766..65987574hg19UCSC Ensembl
Cytoband10q21.3
Allele length
AssemblyAllele length
hg385807
hg195807
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv137e214
Supporting Variantsessv13836199
SamplesNA21135
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623521
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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