A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3539962



Internal ID18741038
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:72442339..72442449hg38UCSC Ensembl
Outerchr6:72442330..72442452hg38UCSC Ensembl
Innerchr6:73152041..73152151hg19UCSC Ensembl
Outerchr6:73152032..73152154hg19UCSC Ensembl
Cytoband6q13
Allele length
AssemblyAllele length
hg38123
hg19123
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9738709
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3539962
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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