A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3597483



Internal ID6984624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:115961316..115962507hg38UCSC Ensembl
Innerchr3:115961342..115962482hg38UCSC Ensembl
Outerchr3:115961291..115962533hg38UCSC Ensembl
chr3:115680163..115681354hg19UCSC Ensembl
Innerchr3:115680189..115681329hg19UCSC Ensembl
Outerchr3:115680138..115681380hg19UCSC Ensembl
Cytoband3q13.31
Allele length
AssemblyAllele length
hg381192
hg191192
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11111205
SamplesHG02272
Known GenesLSAMP
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3597483
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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