A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9765953



Internal ID18740199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:6277125..6277365hg38UCSC Ensembl
Outerchr6:6277068..6277421hg38UCSC Ensembl
Innerchr6:6277358..6277598hg19UCSC Ensembl
Outerchr6:6277301..6277654hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg38354
hg19354
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567206
Supporting Variants
Samples
Known GenesF13A1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9765953
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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