A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9742105



Internal ID18716351
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr8:36213032..36219213hg38UCSC Ensembl
Outerchr8:36212483..36220161hg38UCSC Ensembl
Innerchr8:36070550..36076731hg19UCSC Ensembl
Outerchr8:36070001..36077679hg19UCSC Ensembl
Cytoband8p12
Allele length
AssemblyAllele length
hg387679
hg197679
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3543358
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9742105
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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