A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739370



Internal ID18713616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:149480917..149481744hg38UCSC Ensembl
Outerchr6:149480745..149481765hg38UCSC Ensembl
Innerchr6:149802053..149802880hg19UCSC Ensembl
Outerchr6:149801881..149802901hg19UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381021
hg191021
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540623
Supporting Variants
Samples
Known GenesZC3H12D
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739370
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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