A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9747456



Internal ID18721702
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr12:7883662..7951949hg38UCSC Ensembl
Outerchr12:7882905..7957904hg38UCSC Ensembl
Innerchr12:8036258..8104545hg19UCSC Ensembl
Outerchr12:8035501..8110500hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3875000
hg1975000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3548709
Supporting Variants
Samples
Known GenesSLC2A14, SLC2A3
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9747456
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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