A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739363



Internal ID18713609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149177763..149178002hg38UCSC Ensembl
Outerchr6:149177703..149178058hg38UCSC Ensembl
Innerchr6:149498899..149499138hg19UCSC Ensembl
Outerchr6:149498839..149499194hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540616
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739363
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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