A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9738709



Internal ID18712897
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 StatusS
Merged Variantsesv3539962
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9738709
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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