A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9766024



Internal ID18740270
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:11555877..11556174hg38UCSC Ensembl
Outerchr6:11555820..11556197hg38UCSC Ensembl
Innerchr6:11556110..11556407hg19UCSC Ensembl
Outerchr6:11556053..11556430hg19UCSC Ensembl
Cytoband6p24.2
Allele length
AssemblyAllele length
hg38378
hg19378
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3567277
Supporting Variants
Samples
Known GenesTMEM170B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9766024
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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