A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9751036



Internal ID18725282
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:9652314..9652376hg38UCSC Ensembl
Outerchr2:9652312..9652377hg38UCSC Ensembl
Innerchr2:9792443..9792505hg19UCSC Ensembl
Outerchr2:9792441..9792506hg19UCSC Ensembl
Cytoband2p25.1
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3552289
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9751036
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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