A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3548886



Internal ID18403276
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:23642850..23643098hg38UCSC Ensembl
Outerchr12:23642785..23643131hg38UCSC Ensembl
Innerchr12:23795784..23796032hg19UCSC Ensembl
Outerchr12:23795719..23796065hg19UCSC Ensembl
Cytoband12p12.1
Allele length
AssemblyAllele length
hg38347
hg19347
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9747633
Samples
Known GenesSOX5
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)esv3548886
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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