A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9756096



Internal ID18730342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:62992194..62993791hg38UCSC Ensembl
Outerchr20:62992162..62993901hg38UCSC Ensembl
Innerchr20:61623546..61625143hg19UCSC Ensembl
Outerchr20:61623514..61625253hg19UCSC Ensembl
Cytoband20q13.33
Allele length
AssemblyAllele length
hg381740
hg191740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3557349
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9756096
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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