A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9747590



Internal ID18721836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:19042855..19042916hg38UCSC Ensembl
chr12:19195789..19195850hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3862
hg1962
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548843
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9747590
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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