A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25799806



Internal ID19170622
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:8597882..8680359hg38UCSC Ensembl
Innerchr3:8639568..8722045hg19UCSC Ensembl
Innerchr3:8614568..8697045hg18UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3882478
hg1982478
hg1882478
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893661
Supporting Variants
Samples
Known GenesSSUH2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=31
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25799806
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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