A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3893792



Internal ID18837926
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159110854..159167887hg38UCSC Ensembl
Outerchr3:159110854..159167887hg38UCSC Ensembl
Innerchr3:158828643..158885676hg19UCSC Ensembl
Outerchr3:158828643..158885676hg19UCSC Ensembl
Innerchr3:160311337..160368370hg18UCSC Ensembl
Outerchr3:160311337..160368370hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3857034
hg1957034
hg1857034
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25778576
Samples
Known GenesIQCJ, IQCJ-SCHIP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3893792
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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