A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765924



Internal ID18740170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:3619013..3621627hg38UCSC Ensembl
Outerchr6:3618891..3621734hg38UCSC Ensembl
Innerchr6:3619247..3621861hg19UCSC Ensembl
Outerchr6:3619125..3621968hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg382844
hg192844
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567177
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765924
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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