A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598395



Internal ID6985531
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:160943989..160949564hg38UCSC Ensembl
Innerchr3:160943989..160949564hg38UCSC Ensembl
Outerchr3:160943763..160949711hg38UCSC Ensembl
chr3:160661777..160667352hg19UCSC Ensembl
Innerchr3:160661777..160667352hg19UCSC Ensembl
Outerchr3:160661551..160667499hg19UCSC Ensembl
Cytoband3q25.33
Allele length
AssemblyAllele length
hg385576
hg195576
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11199940, essv11199938, essv11199939
SamplesHG01602, HG01177, HG01069
Known GenesPPM1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598395
Frequency
Sample Size2504
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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