A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25779611



Internal ID18813976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151828253hg38UCSC Ensembl
Innerchr3:151514590..151546041hg19UCSC Ensembl
Innerchr3:152997280..153028731hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3831452
hg1931452
hg1831452
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893786
Supporting Variants
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=20
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25779611
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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