A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766206



Internal ID18740452
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:110722308..110722456hg38UCSC Ensembl
Outerchr1:110722303..110722466hg38UCSC Ensembl
Innerchr1:111264930..111265078hg19UCSC Ensembl
Outerchr1:111264925..111265088hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg38164
hg19164
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567459
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766206
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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