A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595744



Internal ID6983062
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:31026757..31029364hg38UCSC Ensembl
Innerchr3:31026907..31029214hg38UCSC Ensembl
Outerchr3:31026607..31029514hg38UCSC Ensembl
chr3:31068249..31070856hg19UCSC Ensembl
Innerchr3:31068399..31070706hg19UCSC Ensembl
Outerchr3:31068099..31071006hg19UCSC Ensembl
Cytoband3p23
Allele length
AssemblyAllele length
hg382608
hg192608
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10969141, essv10969139, essv10969140, essv10969138
SamplesHG02890, HG03057, HG03054, HG03575
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595744
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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