A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598371



Internal ID6985507
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159735046..159736035hg38UCSC Ensembl
Innerchr3:159735079..159736003hg38UCSC Ensembl
Outerchr3:159735014..159736068hg38UCSC Ensembl
chr3:159452835..159453824hg19UCSC Ensembl
Innerchr3:159452868..159453792hg19UCSC Ensembl
Outerchr3:159452803..159453857hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg38990
hg19990
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199565, essv11199563, essv11199566, essv11199564
SamplesHG03575, HG03240, HG02983, HG03470
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598371
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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