A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598987



Internal ID6986035
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:186182160..186184452hg38UCSC Ensembl
Innerchr3:186182160..186184452hg38UCSC Ensembl
Outerchr3:186181965..186184638hg38UCSC Ensembl
chr3:185899949..185902241hg19UCSC Ensembl
Innerchr3:185899949..185902241hg19UCSC Ensembl
Outerchr3:185899754..185902427hg19UCSC Ensembl
Cytoband3q27.2
Allele length
AssemblyAllele length
hg382293
hg192293
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11257996, essv11257997
SamplesNA18582, HG03303
Known GenesDGKG
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598987
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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