A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623208



Internal ID6663376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:50507575..50512979hg38UCSC Ensembl
Innerchr10:50507586..50512968hg38UCSC Ensembl
Outerchr10:50507564..50512990hg38UCSC Ensembl
chr10:52267335..52272739hg19UCSC Ensembl
Innerchr10:52267346..52272728hg19UCSC Ensembl
Outerchr10:52267324..52272750hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg385405
hg195405
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv128e214
Supporting Variantsessv13803074, essv13803075
SamplesNA21133, HG03931
Known GenesSGMS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623208
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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