A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25778576



Internal ID18818140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:159110854..159167887hg38UCSC Ensembl
Innerchr3:158828643..158885676hg19UCSC Ensembl
Innerchr3:160311337..160368370hg18UCSC Ensembl
Cytoband3q25.32
Allele length
AssemblyAllele length
hg3857034
hg1957034
hg1857034
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893792
Supporting Variants
Samples
Known GenesIQCJ, IQCJ-SCHIP1
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=9
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25778576
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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