A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598373



Internal ID6638639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:159763144..159768738hg38UCSC Ensembl
Innerchr3:159763144..159768738hg38UCSC Ensembl
Outerchr3:159763091..159768756hg38UCSC Ensembl
chr3:159480933..159486527hg19UCSC Ensembl
Innerchr3:159480933..159486527hg19UCSC Ensembl
Outerchr3:159480880..159486545hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385595
hg195595
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199571, essv11199569, essv11199570, essv11199568
SamplesHG00142, HG00306, HG01945, HG00311
Known GenesIQCJ-SCHIP1, SCHIP1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598373
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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