A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9747754



Internal ID18722000
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:31620811..31621054hg38UCSC Ensembl
Outerchr12:31620767..31621122hg38UCSC Ensembl
Innerchr12:31773745..31773988hg19UCSC Ensembl
Outerchr12:31773701..31774056hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38356
hg19356
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3549007
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9747754
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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