A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3596541



Internal ID6983855
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:72711717..72718468hg38UCSC Ensembl
chr3:72760868..72767619hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg386752
hg196752
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11038692, essv11038688, essv11038690, essv11038689, essv11038691
SamplesNA19020, NA20359, NA19320, NA19452, NA20362
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3596541
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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