A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623216



Internal ID6663384
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50870487..50871121hg38UCSC Ensembl
Innerchr10:50870487..50871121hg38UCSC Ensembl
Outerchr10:50870234..50871363hg38UCSC Ensembl
chr10:52630247..52630881hg19UCSC Ensembl
Innerchr10:52630247..52630881hg19UCSC Ensembl
Outerchr10:52629994..52631123hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg38635
hg19635
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13803445
SamplesHG00158
Known GenesA1CF
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623216
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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