A curated catalogue of human genomic structural variation




Variant Details

Variant: essv25784699



Internal ID19165940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:114923561..114949049hg38UCSC Ensembl
Innerchr3:114642408..114667896hg19UCSC Ensembl
Innerchr3:116125098..116150586hg18UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg3825489
hg1925489
hg1825489
Variant TypeCNV loss
Copy Number1
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3893769
Supporting Variants
Samples
Known GenesZBTB20
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
CommentsNumber of probes=7
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)essv25784699
Frequency
Sample Size3017
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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