A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893786



Internal ID18837920
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:151796802..151828253hg38UCSC Ensembl
Outerchr3:151796802..151828253hg38UCSC Ensembl
Innerchr3:151514590..151546041hg19UCSC Ensembl
Outerchr3:151514590..151546041hg19UCSC Ensembl
Innerchr3:152997280..153028731hg18UCSC Ensembl
Outerchr3:152997280..153028731hg18UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg3831452
hg1931452
hg1831452
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25786855, essv25780152, essv25778878, essv25779611
Samples
Known GenesAADAC, MIR548H2
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893786
Frequency
Sample Size3017
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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