A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3546672



Internal ID18747748
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:91055675..91055934hg38UCSC Ensembl
Outerchr10:91055614..91055993hg38UCSC Ensembl
Innerchr10:92815432..92815691hg19UCSC Ensembl
Outerchr10:92815371..92815750hg19UCSC Ensembl
Cytoband10q23.31
Allele length
AssemblyAllele length
hg38380
hg19380
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9745419
Samples
Known GenesLINC00502
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3546672
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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