A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598292



Internal ID6638558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:155991305..156053874hg38UCSC Ensembl
chr3:155709094..155771663hg19UCSC Ensembl
Cytoband3q25.31
Allele length
AssemblyAllele length
hg3862570
hg1962570
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11191929
SamplesNA21088
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598292
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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