A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595904



Internal ID6983222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:37959533..37960545hg38UCSC Ensembl
Innerchr3:37959583..37960495hg38UCSC Ensembl
Outerchr3:37959469..37960609hg38UCSC Ensembl
chr3:38001024..38002036hg19UCSC Ensembl
Innerchr3:38001074..38001986hg19UCSC Ensembl
Outerchr3:38000960..38002100hg19UCSC Ensembl
Cytoband3p22.2
Allele length
AssemblyAllele length
hg381013
hg191013
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10983703
SamplesHG02410
Known GenesCTDSPL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595904
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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