A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598728



Internal ID6985863
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:174439686..174443793hg38UCSC Ensembl
Innerchr3:174439686..174443793hg38UCSC Ensembl
Outerchr3:174439600..174443845hg38UCSC Ensembl
chr3:174157476..174161583hg19UCSC Ensembl
Innerchr3:174157476..174161583hg19UCSC Ensembl
Outerchr3:174157390..174161635hg19UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg384108
hg194108
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11229684
SamplesNA20503
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598728
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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