A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766258



Internal ID18393818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:30918661..30918789hg38UCSC Ensembl
Outerchr6:30918653..30918797hg38UCSC Ensembl
Innerchr6:30886438..30886566hg19UCSC Ensembl
Outerchr6:30886430..30886574hg19UCSC Ensembl
Cytoband6p21.33
Allele length
AssemblyAllele length
hg38145
hg19145
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567511
Supporting Variants
Samples
Known GenesVARS2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766258
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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