A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9739332



Internal ID18713578
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:143875482..143878093hg38UCSC Ensembl
Outerchr6:143875193..143878743hg38UCSC Ensembl
Innerchr6:144196619..144199230hg19UCSC Ensembl
Outerchr6:144196330..144199880hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg383551
hg193551
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3540585
Supporting Variants
Samples
Known GenesZC2HC1B
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9739332
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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