A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742626



Internal ID18716872
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:95521492..95521573hg38UCSC Ensembl
chr8:96533720..96533801hg19UCSC Ensembl
Cytoband8q22.1
Allele length
AssemblyAllele length
hg3882
hg1982
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543879
Supporting Variants
Samples
Known GenesLOC100616530
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742626
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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